A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522996



Internal ID15450289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78883471..78900074hg38UCSC Ensembl
Innerchr15:79175813..79192416hg19UCSC Ensembl
Innerchr15:76962868..76979471hg18UCSC Ensembl
Innerchr15:76962868..76979471hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3816604
hg1916604
hg1816604
hg1716604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698666
Samples
Known GenesMORF4L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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