A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526244



Internal ID15453537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:239608154..239611370hg38UCSC Ensembl
Innerchr1:239771454..239774670hg19UCSC Ensembl
Innerchr1:237838077..237841293hg18UCSC Ensembl
Innerchr1:236097495..236100711hg17UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg383217
hg193217
hg183217
hg173217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702516
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526244
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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