A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065296



Internal ID18807827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58704294..58803955hg38UCSC Ensembl
Innerchr16:58738198..58837859hg19UCSC Ensembl
Innerchr16:57295699..57395360hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3899662
hg1999662
hg1899662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722717
Samples
Known GenesGOT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065296
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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