A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174250



Internal ID15508829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71302291..71340509hg38UCSC Ensembl
Innerchr10:73062048..73100266hg19UCSC Ensembl
Innerchr10:72732054..72770272hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3838219
hg1938219
hg1838219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551500
Supporting Variants
Samples1782681092_A
Known GenesSLC29A3, UNC5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174250
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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