A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044582



Internal ID18787113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15893399..15930167hg38UCSC Ensembl
Innerchr16:15987256..16024024hg19UCSC Ensembl
Innerchr16:15894757..15931525hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3836769
hg1936769
hg1836769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2773n100
Supporting Variantsnssv3557985, nssv3557986
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)nsv1044582
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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