A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654999



Internal ID15044965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34480941..34506197hg38UCSC Ensembl
Innerchr19:34971846..34997102hg19UCSC Ensembl
Innerchr19:39663686..39688942hg18UCSC Ensembl
Innerchr19:39663686..39688942hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3825257
hg1925257
hg1825257
hg1725257
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517392
Supporting Variants
Samples
Known GenesWTIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654999
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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