A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743479



Internal ID15690749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5670347..5693685hg38UCSC Ensembl
Innerchr10:5712310..5735648hg19UCSC Ensembl
Innerchr10:5752316..5775654hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3823339
hg1923339
hg1823339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549895
Supporting Variants
Samples
Known GenesFAM208B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv743479
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