A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155606



Internal ID22086111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51639362..51644944hg38UCSC Ensembl
Outerchr19:51639099..51651652hg38UCSC Ensembl
Innerchr19:52142615..52148197hg19UCSC Ensembl
Outerchr19:52142352..52154905hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3812554
hg1912554
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013673, nssv4015077, nssv4013679, nssv4013686, nssv4013667, nssv4015066, nssv4015050, nssv4013672, nssv4015057, nssv4015090, nssv4015084, nssv4013680, nssv4013683, nssv4013678, nssv4015082, nssv4015081, nssv4015083, nssv4013675, nssv4015099, nssv4015101, nssv4013687, nssv4015097, nssv4013668, nssv4015080, nssv4013682, nssv4013669, nssv4015079, nssv4015087, nssv4015069, nssv4013688, nssv4013681, nssv4015093, nssv4015067, nssv4015053, nssv4015100, nssv4013665, nssv4015054, nssv4013666, nssv4015092, nssv4013671, nssv4015056, nssv4015078, nssv4015072, nssv4013677, nssv4015098, nssv4015049, nssv4015076, nssv4015055, nssv4015071, nssv4015062, nssv4015061, nssv4015043, nssv4015089, nssv4015045, nssv4015085, nssv4013674, nssv4013670, nssv4015048, nssv4013676, nssv4013664, nssv4015091, nssv4015095, nssv4015088, nssv4015068, nssv4015047, nssv4015070, nssv4015060, nssv4015058, nssv4015064, nssv4015044, nssv4015046, nssv4015086, nssv4015063, nssv4015096, nssv4015052, nssv4013684, nssv4015073, nssv4015075, nssv4015074, nssv4015059, nssv4013685, nssv4015065, nssv4015051
Samples
Known GenesSIGLEC14
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155606
Frequency
Sample Size131
Observed Gain7
Observed Loss76
Observed Complex0
Frequencyn/a


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