A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667681



Internal ID15057647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44347982..44365553hg38UCSC Ensembl
Innerchr19:44852134..44869713hg19UCSC Ensembl
Innerchr19:49543974..49561553hg18UCSC Ensembl
Innerchr19:49543974..49561553hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3817572
hg1917580
hg1817580
hg1717580
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515911
Supporting Variants
Samples
Known GenesZNF112
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667681
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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