A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693634



Internal ID15430286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19737676..19760441hg38UCSC Ensembl
Innerchr19:19848485..19871250hg19UCSC Ensembl
Innerchr19:19709485..19732250hg18UCSC Ensembl
Innerchr19:19709485..19732250hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3822766
hg1922766
hg1822766
hg1722766
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517362
Supporting Variants
Samples
Known GenesLINC00663
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693634
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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