A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526014



Internal ID15106621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80044884..80150694hg38UCSC Ensembl
Innerchr15:80337226..80443036hg19UCSC Ensembl
Innerchr15:78124281..78230091hg18UCSC Ensembl
Innerchr15:78124281..78230091hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38105811
hg19105811
hg18105811
hg17105811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702242
Samples
Known GenesZFAND6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526014
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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