A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059932



Internal ID19149151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..32233151hg38UCSC Ensembl
Innerchr16:32058483..32244472hg19UCSC Ensembl
Innerchr16:31965984..32151973hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38185990
hg19185990
hg18185990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549259
Samples
Known GenesHERC2P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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