A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740167



Internal ID15687437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1019000..1027744hg38UCSC Ensembl
Innerchr10:1064940..1073684hg19UCSC Ensembl
Innerchr10:1054940..1063684hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg388745
hg198745
hg188745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549767
Supporting Variants
Samples
Known GenesIDI2, IDI2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv740167
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