A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664610



Internal ID15054576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34480941..34496475hg38UCSC Ensembl
Innerchr19:34971846..34987380hg19UCSC Ensembl
Innerchr19:39663686..39679220hg18UCSC Ensembl
Innerchr19:39663686..39679220hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3815535
hg1915535
hg1815535
hg1715535
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)nssv664610
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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