A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549770



Internal ID15990493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1237304..1240317hg38UCSC Ensembl
Innerchr10:1281436..1282332hg19UCSC Ensembl
Innerchr10:1271436..1272332hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383014
hg19897
hg18897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv927n54
Supporting Variantsnssv740171, nssv740174, nssv740173, nssv740172
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549770
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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