A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515990



Internal ID15096597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6489014..6501574hg38UCSC Ensembl
Innerchr11:6510244..6522804hg19UCSC Ensembl
Innerchr11:6466820..6479380hg18UCSC Ensembl
Innerchr11:6466820..6479380hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812561
hg1912561
hg1812561
hg1712561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665607, nssv669741, nssv703812
Samples
Known GenesDNHD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515990
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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