A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569602



Internal ID16010325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58622127..58672238hg38UCSC Ensembl
Innerchr15:58914326..58964437hg19UCSC Ensembl
Innerchr15:56701618..56751729hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3850112
hg1950112
hg1850112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843580
Samples
Known GenesADAM10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569602
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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