A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699230



Internal ID15435882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20324851..20614838hg38UCSC Ensembl
Innerchr19:20435660..20797644hg19UCSC Ensembl
Innerchr19:20296660..20589484hg18UCSC Ensembl
Innerchr19:20296660..20589484hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38289988
hg19361985
hg18292825
hg17292825
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523471
Supporting Variants
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF737, ZNF826P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699230
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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