A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517357



Internal ID15097964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44250972..44271979hg38UCSC Ensembl
Innerchr11:44272522..44293529hg19UCSC Ensembl
Innerchr11:44229098..44250105hg18UCSC Ensembl
Innerchr11:44229098..44250105hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3821008
hg1921008
hg1821008
hg1721008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv67n21
Supporting Variantsnssv651808, nssv673390, nssv697802, nssv669788, nssv656695, nssv679889, nssv665488, nssv673303, nssv671368, nssv705210, nssv656877, nssv687101, nssv663276
Samples
Known GenesALX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517357
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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