A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747533



Internal ID16041489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46379977hg38UCSC Ensembl
Innerchr10:47543322..47751237hg19UCSC Ensembl
Innerchr10:47013328..47221243hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38207892
hg19207916
hg18207916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550760
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)nssv747533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer