A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746836



Internal ID15694106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34786889..34974998hg38UCSC Ensembl
Innerchr10:35075817..35263926hg19UCSC Ensembl
Innerchr10:35115823..35303932hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38188110
hg19188110
hg18188110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550397
Supporting Variants
Samples
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746836
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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