A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1036462



Internal ID15889648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90962767..91006300hg38UCSC Ensembl
Innerchr5:90258584..90302117hg19UCSC Ensembl
Innerchr5:90294340..90337873hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3843534
hg1943534
hg1843534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598929
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)nssv1036462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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