A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv740222



Internal ID15687492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1549641..1568644hg38UCSC Ensembl
Innerchr10:1591836..1610839hg19UCSC Ensembl
Innerchr10:1581836..1600839hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3819004
hg1919004
hg1819004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549792
Supporting Variants
Samples
Known GenesADARB2, ADARB2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv740222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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