A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523596



Internal ID15450889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142413907..142445893hg38UCSC Ensembl
Innerchr3:142132749..142164735hg19UCSC Ensembl
Innerchr3:143615439..143647425hg18UCSC Ensembl
Innerchr3:143615447..143647433hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3831987
hg1931987
hg1831987
hg1731987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699388
Samples
Known GenesXRN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523596
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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