A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571515



Internal ID16012238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14697797..14742768hg38UCSC Ensembl
Innerchr16:14791654..14836625hg19UCSC Ensembl
Innerchr16:14699155..14744126hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3844972
hg1944972
hg1844972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4916n54
Supporting Variantsnssv852786
Samples
Known GenesNPIPA2, NPIPA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571515
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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