A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527793



Internal ID15455086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:104960113..105812628hg38UCSC Ensembl
Innerchr10:106719871..107572386hg19UCSC Ensembl
Innerchr10:106709861..107562376hg18UCSC Ensembl
Innerchr10:106709861..107562376hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38852516
hg19852516
hg18852516
hg17852516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704285
Samples
Known GenesSORCS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527793
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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