A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859127



Internal ID16153083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72057644..72059728hg38UCSC Ensembl
Innerchr16:72091543..72093627hg19UCSC Ensembl
Innerchr16:70649044..70651128hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg382085
hg192085
hg182085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572953
Supporting Variants
Samples
Known GenesHP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859127
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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