A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057765



Internal ID19146984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88382623..88424550hg38UCSC Ensembl
Innerchr16:88449031..88490958hg19UCSC Ensembl
Innerchr16:86976532..87018459hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3841928
hg1941928
hg1841928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3063n100
Supporting Variantsnssv3559988, nssv3559986, nssv3559987
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)nsv1057765
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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