A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861938



Internal ID16155894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81557891..81577117hg38UCSC Ensembl
Innerchr16:81591496..81610722hg19UCSC Ensembl
Innerchr16:80148997..80168223hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3819227
hg1919227
hg1819227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573361
Supporting Variants
Samples
Known GenesCMIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861938
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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