A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568804



Internal ID16356213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483278..31483974hg38UCSC Ensembl
Innerchr15:31775481..31776177hg19UCSC Ensembl
Innerchr15:29562773..29563469hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38697
hg19697
hg18697
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4436n54
Supporting Variantsnssv839581, nssv839580
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568804
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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