A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149171



Internal ID15880460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60035366..60114910hg38UCSC Ensembl
Innerchr16:60069270..60148814hg19UCSC Ensembl
Innerchr16:58626771..58706315hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3879545
hg1979545
hg1879545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572834
Supporting Variants
SamplesNINDS_212
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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