A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526729



Internal ID15107336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25643543..25706319hg38UCSC Ensembl
Innerchr4:25645165..25707941hg19UCSC Ensembl
Innerchr4:25254263..25317039hg18UCSC Ensembl
Innerchr4:25321434..25384210hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3862777
hg1962777
hg1862777
hg1762777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703070
Samples
Known GenesSLC34A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526729
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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