A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747635



Internal ID15694905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46259024..46332377hg38UCSC Ensembl
Innerchr10:47630260..47703613hg19UCSC Ensembl
Innerchr10:47100266..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3873354
hg1973354
hg1873354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550795
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747635
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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