A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149326



Internal ID15529185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83817468..83908216hg38UCSC Ensembl
Innerchr16:83851073..83941821hg19UCSC Ensembl
Innerchr16:82408574..82499322hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3890749
hg1990749
hg1890749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573406
Supporting Variants
SamplesHGDP00748
Known GenesMLYCD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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