A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052538



Internal ID19141757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28791224..28816923hg38UCSC Ensembl
Innerchr10:29080153..29105852hg19UCSC Ensembl
Innerchr10:29120159..29145858hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3825700
hg1925700
hg1825700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514994
Samples
Known GenesLINC00837
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052538
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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