A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526514



Internal ID15453807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132177951..132180333hg38UCSC Ensembl
Innerchr7:131862710..131865092hg19UCSC Ensembl
Innerchr7:131513250..131515632hg18UCSC Ensembl
Innerchr7:131319965..131322347hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382383
hg192383
hg182383
hg172383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702824
Samples
Known GenesPLXNA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526514
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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