A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524269



Internal ID15104876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86654455..86680809hg38UCSC Ensembl
Innerchr10:88414212..88440566hg19UCSC Ensembl
Innerchr10:88404192..88430546hg18UCSC Ensembl
Innerchr10:88404192..88430546hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3826355
hg1926355
hg1826355
hg1726355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700167
Samples
Known GenesLDB3, OPN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524269
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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