A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149276



Internal ID15879872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:605686..670986hg38UCSC Ensembl
Innerchr16:655686..720986hg19UCSC Ensembl
Innerchr16:595687..660987hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3865301
hg1965301
hg1865301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571013
Supporting Variants
SamplesNINDS_119
Known GenesC16orf13, FAM195A, RAB40C, RHOT2, WDR90, WFIKKN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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