A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549774



Internal ID15990497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1237571..1240183hg38UCSC Ensembl
Innerchr10:1281487..1282221hg19UCSC Ensembl
Innerchr10:1271487..1272221hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382613
hg19735
hg18735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv926n54
Supporting Variantsnssv740179
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549774
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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