A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149660



Internal ID15507828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77694338..77976550hg38UCSC Ensembl
Innerchr16:77728235..78010447hg19UCSC Ensembl
Innerchr16:76285736..76567948hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38282213
hg19282213
hg18282213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573129
Supporting Variants
Samples1780862176_A
Known GenesNUDT7, VAT1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149660
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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