A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549787



Internal ID15990510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1300624..1301363hg38UCSC Ensembl
Innerchr10:1342819..1343558hg19UCSC Ensembl
Innerchr10:1332819..1333558hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38740
hg19740
hg18740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740216
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549787
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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