A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061872



Internal ID19151091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35431547hg38UCSC Ensembl
Innerchr17:33684107..33758566hg19UCSC Ensembl
Innerchr17:30708220..30782679hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3874460
hg1974460
hg1874460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n100
Supporting Variantsnssv3561097, nssv3561089, nssv3561098, nssv3720045, nssv3561078, nssv3561092, nssv3561084, nssv3720054, nssv3720047, nssv3561096, nssv3561099, nssv3561100, nssv3561094, nssv3561088, nssv3561093, nssv3720053, nssv3561086, nssv3561083, nssv3720050, nssv3561082, nssv3720051, nssv3561095, nssv3561091, nssv3561087, nssv3561081, nssv3561090, nssv3561085, nssv3720048, nssv3561079, nssv3561080, nssv3720049, nssv3720052, nssv3720046
Samples
Known GenesSLFN11, SLFN12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061872
Frequency
Sample Size11257
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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