A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528426



Internal ID15455719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152189259..152189630hg38UCSC Ensembl
Innerchr1:152161735..152162106hg19UCSC Ensembl
Innerchr1:150428359..150428730hg18UCSC Ensembl
Innerchr1:148974808..148975179hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38372
hg19372
hg18372
hg17372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705019
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528426
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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