A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516033



Internal ID15443090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11130765..11137550hg38UCSC Ensembl
Innerchr8:10988275..10995060hg19UCSC Ensembl
Innerchr8:11025685..11032470hg18UCSC Ensembl
Innerchr8:11025685..11032470hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386786
hg196786
hg186786
hg176786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696486, nssv678931, nssv690422, nssv661798, nssv657372, nssv659548, nssv665830, nssv674811, nssv685502, nssv668030, nssv688056, nssv672434, nssv675573
Samples
Known GenesXKR6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516033
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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