A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747639



Internal ID15694909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46316565..46370665hg38UCSC Ensembl
Innerchr10:47687801..47741882hg19UCSC Ensembl
Innerchr10:47157807..47211888hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3854101
hg1954082
hg1854082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550799
Supporting Variants
Samples
Known GenesANTXRL, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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