A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526805



Internal ID15107412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:37899158..37899532hg38UCSC Ensembl
Innerchr4:37900779..37901153hg19UCSC Ensembl
Innerchr4:37577174..37577548hg18UCSC Ensembl
Innerchr4:37723345..37723719hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38375
hg19375
hg18375
hg17375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703159
Samples
Known GenesTBC1D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526805
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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