A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570776



Internal ID16011499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99965534..100191914hg38UCSC Ensembl
Innerchr15:100505739..100732119hg19UCSC Ensembl
Innerchr15:98323262..98549642hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38226381
hg19226381
hg18226381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv850862
Samples
Known GenesADAMTS17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570776
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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