A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057264



Internal ID19146483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65332087..65450341hg38UCSC Ensembl
Innerchr16:65365990..65484244hg19UCSC Ensembl
Innerchr16:63923491..64041745hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38118255
hg19118255
hg18118255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2994n100
Supporting Variantsnssv3559438
Samples
Known GenesLINC00922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057264
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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