A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515568



Internal ID15443179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167917136..168208655hg38UCSC Ensembl
Innerchr6:168317816..168609335hg19UCSC Ensembl
Innerchr6:168060665..168352184hg18UCSC Ensembl
Innerchr6:168136372..168427891hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38291520
hg19291520
hg18291520
hg17291520
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676241, nssv701335, nssv655977, nssv688132, nssv668141, nssv682244, nssv664114, nssv679985, nssv674061, nssv671628, nssv654873, nssv670545, nssv663929, nssv701625, nssv666706, nssv666881, nssv666637, nssv678176, nssv693442, nssv700319, nssv689118, nssv681569, nssv667552, nssv694840, nssv696820, nssv667298, nssv669582, nssv685952
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515568
Frequency
Sample Size2026
Observed Gain19
Observed Loss9
Observed Complex0
Frequencyn/a


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