A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747423



Internal ID15694693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46292460hg38UCSC Ensembl
Innerchr10:47543322..47663696hg19UCSC Ensembl
Innerchr10:47013328..47133702hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38120375
hg19120375
hg18120375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550746
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)nssv747423
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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