A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526945



Internal ID15107552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45643557..45649491hg38UCSC Ensembl
Innerchr15:45935755..45941689hg19UCSC Ensembl
Innerchr15:43723047..43728981hg18UCSC Ensembl
Innerchr15:43723047..43728981hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385935
hg195935
hg185935
hg175935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703315
Samples
Known GenesSQRDL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526945
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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