A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038616



Internal ID19127835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7799222..8064253hg38UCSC Ensembl
Innerchr16:7849224..8114255hg19UCSC Ensembl
Innerchr16:7789225..8054256hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38265032
hg19265032
hg18265032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2720n100
Supporting Variantsnssv3557091
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038616
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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