A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519358



Internal ID15446651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38205734..38207571hg38UCSC Ensembl
Innerchr1:38671406..38673243hg19UCSC Ensembl
Innerchr1:38443993..38445830hg18UCSC Ensembl
Innerchr1:38340499..38342336hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381838
hg191838
hg181838
hg171838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694325
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519358
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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