A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570777



Internal ID16011500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99970220..100379252hg38UCSC Ensembl
Innerchr15:100510425..100919457hg19UCSC Ensembl
Innerchr15:98327948..98736980hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38409033
hg19409033
hg18409033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv850863
Samples
Known GenesADAMTS17, SPATA41
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570777
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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