A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1036463



Internal ID15889649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90962767..91007947hg38UCSC Ensembl
Innerchr5:90258584..90303764hg19UCSC Ensembl
Innerchr5:90294340..90339520hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3845181
hg1945181
hg1845181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598930
Supporting Variants
Samples
Known GenesGPR98
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1036463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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