A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570531



Internal ID16011254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:94238675..94285237hg38UCSC Ensembl
Innerchr15:94781904..94828466hg19UCSC Ensembl
Innerchr15:92582908..92629470hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3846563
hg1946563
hg1846563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4730n54
Supporting Variantsnssv848957
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570531
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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