A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711303



Internal ID16005259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22563356..22564322hg38UCSC Ensembl
Innerchr1:22889849..22890815hg19UCSC Ensembl
Innerchr1:22762436..22763402hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38967
hg19967
hg18967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545754
Supporting Variants
Samples
Known GenesEPHA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711303
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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