A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037882



Internal ID19127101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19929929..19951789hg38UCSC Ensembl
Innerchr16:19941251..19963111hg19UCSC Ensembl
Innerchr16:19848752..19870612hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3821861
hg1921861
hg1821861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2788n100
Supporting Variantsnssv3542776
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)nsv1037882
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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