A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524107



Internal ID15104714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76167798..76170678hg38UCSC Ensembl
Innerchr10:77927556..77930436hg19UCSC Ensembl
Innerchr10:77597562..77600442hg18UCSC Ensembl
Innerchr10:77597562..77600442hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382881
hg192881
hg182881
hg172881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699985
Samples
Known GenesC10orf11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524107
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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