A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549767



Internal ID15990490
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 StatusM
Merged Variants
Supporting Variantsnssv740167, nssv740166, nssv740168
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)nsv549767
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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