A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705810



Internal ID15095776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11192131..11216950hg38UCSC Ensembl
Innerchr19:11302807..11327626hg19UCSC Ensembl
Innerchr19:11163807..11188626hg18UCSC Ensembl
Innerchr19:11163807..11188626hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824820
hg1924820
hg1824820
hg1724820
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522449
Supporting Variants
Samples
Known GenesDOCK6, KANK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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