A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054432



Internal ID18796963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1069686..1184491hg38UCSC Ensembl
Innerchr10:1115626..1230431hg19UCSC Ensembl
Innerchr10:1105626..1220431hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38114806
hg19114806
hg18114806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502624
Samples
Known GenesADARB2, LINC00200, WDR37
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054432
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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