A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523583



Internal ID15104190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14850411..14852902hg38UCSC Ensembl
Innerchr10:14892410..14894901hg19UCSC Ensembl
Innerchr10:14932416..14934907hg18UCSC Ensembl
Innerchr10:14932416..14934907hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382492
hg192492
hg182492
hg172492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699372
Samples
Known GenesHSPA14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523583
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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