A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549798



Internal ID15990521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2031733..2348387hg38UCSC Ensembl
Innerchr10:2073927..2390581hg19UCSC Ensembl
Innerchr10:2063927..2380581hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38316655
hg19316655
hg18316655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740232
Samples
Known GenesLINC00701, MIR6072
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549798
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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