A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515847



Internal ID15096454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11992070..11995398hg38UCSC Ensembl
Innerchr11:12013617..12016945hg19UCSC Ensembl
Innerchr11:11970193..11973521hg18UCSC Ensembl
Innerchr11:11970193..11973521hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg383329
hg193329
hg183329
hg173329
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699259, nssv654912, nssv658142, nssv687787, nssv670981, nssv665113, nssv690012, nssv662310, nssv663639, nssv669088, nssv686440, nssv679637, nssv693824, nssv665005, nssv668660, nssv654604
Samples
Known GenesDKK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515847
Frequency
Sample Size2026
Observed Gain8
Observed Loss8
Observed Complex0
Frequencyn/a


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