A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523379



Internal ID15450672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64610069..64667068hg38UCSC Ensembl
Innerchr10:66369826..66426825hg19UCSC Ensembl
Innerchr10:66039832..66096831hg18UCSC Ensembl
Innerchr10:66039832..66096831hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3857000
hg1957000
hg1857000
hg1757000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699128
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523379
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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