A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520490



Internal ID15447783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155353195..155376740hg38UCSC Ensembl
Innerchr6:155674329..155697874hg19UCSC Ensembl
Innerchr6:155716021..155739566hg18UCSC Ensembl
Innerchr6:155766442..155789987hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3823546
hg1923546
hg1823546
hg1723546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672458, nssv677311, nssv696842, nssv671816, nssv688940
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520490
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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