A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659871



Internal ID15396523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51246983..51254873hg38UCSC Ensembl
Innerchr19:51750238..51758127hg19UCSC Ensembl
Innerchr19:56442050..56449939hg18UCSC Ensembl
Innerchr19:56442050..56449939hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387891
hg197890
hg187890
hg177890
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519982
Supporting Variants
Samples
Known GenesSIGLECL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659871
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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