A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973100



Internal ID15920370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129314893..129344387hg38UCSC Ensembl
Innerchr3:129033736..129063230hg19UCSC Ensembl
Innerchr3:130516426..130545920hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3829495
hg1929495
hg1829495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591651
Supporting Variants
Samples
Known GenesH1FX, H1FX-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv973100
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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