A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701433



Internal ID15091399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57496417..57500053hg38UCSC Ensembl
Innerchr19:58007785..58011421hg19UCSC Ensembl
Innerchr19:62699597..62703233hg18UCSC Ensembl
Innerchr19:62699597..62703233hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383637
hg193637
hg183637
hg173637
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525323
Supporting Variants
Samples
Known GenesZNF773
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701433
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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