A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747531



Internal ID15694801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46377652hg38UCSC Ensembl
Innerchr10:47543322..47748912hg19UCSC Ensembl
Innerchr10:47013328..47218918hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38205567
hg19205591
hg18205591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550758
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1, ANXA8L1, ANXA8L2, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747531
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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