A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv737463



Internal ID15684733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:228151238..228163073hg38UCSC Ensembl
Innerchr1:228338939..228350774hg19UCSC Ensembl
Innerchr1:226405562..226417397hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3811836
hg1911836
hg1811836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549291
Supporting Variants
Samples
Known GenesGJC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv737463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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