A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699631



Internal ID15436283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34943334..34944102hg38UCSC Ensembl
Innerchr19:35434238..35435006hg19UCSC Ensembl
Innerchr19:40126078..40126846hg18UCSC Ensembl
Innerchr19:40126078..40126846hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38769
hg19769
hg18769
hg17769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523802
Supporting Variants
Samples
Known GenesZNF30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699631
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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