A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549785



Internal ID15990508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1238777..1240333hg38UCSC Ensembl
Innerchr10:1281806..1282372hg19UCSC Ensembl
Innerchr10:1271806..1272372hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381557
hg19567
hg18567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv930n54
Supporting Variantsnssv740212, nssv740213, nssv740211, nssv740214
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549785
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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