A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1036464



Internal ID15889650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90962767..91011335hg38UCSC Ensembl
Innerchr5:90258584..90307152hg19UCSC Ensembl
Innerchr5:90294340..90342908hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3848569
hg1948569
hg1848569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598931
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)nssv1036464
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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