A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694451



Internal ID15084417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9290483..9306073hg38UCSC Ensembl
Innerchr19:9401159..9416749hg19UCSC Ensembl
Innerchr19:9262159..9277749hg18UCSC Ensembl
Innerchr19:9262159..9277749hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3815591
hg1915591
hg1815591
hg1715591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521091
Supporting Variants
Samples
Known GenesZNF699
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694451
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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