A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515835



Internal ID15442892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68600650..68604733hg38UCSC Ensembl
Innerchr15:68892989..68897072hg19UCSC Ensembl
Innerchr15:66680043..66684126hg18UCSC Ensembl
Innerchr15:66680043..66684126hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384084
hg194084
hg184084
hg174084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683049, nssv664946
Samples
Known GenesCORO2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515835
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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