A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065634



Internal ID18808165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57638274..57670341hg38UCSC Ensembl
Innerchr16:57672186..57704253hg19UCSC Ensembl
Innerchr16:56229687..56261754hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3832068
hg1932068
hg1832068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559353
Samples
Known GenesGPR56, GPR97
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065634
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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