A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858122



Internal ID15805392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57692334..57695519hg38UCSC Ensembl
Innerchr16:57726246..57729431hg19UCSC Ensembl
Innerchr16:56283747..56286932hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg383186
hg193186
hg183186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572755
Supporting Variants
Samples
Known GenesCCDC135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv858122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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