A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041498



Internal ID18784029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1071260..1717996hg38UCSC Ensembl
Innerchr10:1117200..1760190hg19UCSC Ensembl
Innerchr10:1107200..1750190hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38646737
hg19642991
hg18642991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3488428
Samples
Known GenesADARB2, ADARB2-AS1, 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)nsv1041498
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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