A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174979



Internal ID15877248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34747919..34858486hg38UCSC Ensembl
Innerchr10:35036847..35147414hg19UCSC Ensembl
Innerchr10:35076853..35187420hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38110568
hg19110568
hg18110568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550395
Supporting Variants
SamplesHGDP00956
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174979
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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