A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700183



Internal ID15436835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12075946..12077451hg38UCSC Ensembl
Innerchr19:12186761..12188266hg19UCSC Ensembl
Innerchr19:12047761..12049266hg18UCSC Ensembl
Innerchr19:12047761..12049266hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381506
hg191506
hg181506
hg171506
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524284
Supporting Variants
Samples
Known GenesZNF844
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700183
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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