A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517206



Internal ID15444499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145906839..145942575hg38UCSC Ensembl
Innerchr3:145624626..145660362hg19UCSC Ensembl
Innerchr3:147107316..147143052hg18UCSC Ensembl
Innerchr3:147107324..147143060hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3835737
hg1935737
hg1835737
hg1735737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674258, nssv667407, nssv660838, nssv689514, nssv652201, nssv674098, nssv665363, nssv654010
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517206
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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