A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665270



Internal ID15055236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44398850..44430844hg38UCSC Ensembl
Innerchr19:44903015..44935019hg19UCSC Ensembl
Innerchr19:49594855..49626859hg18UCSC Ensembl
Innerchr19:49594855..49626859hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3831995
hg1932005
hg1832005
hg1732005
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515911
Supporting Variants
Samples
Known GenesZNF229, ZNF285
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665270
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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