A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526757



Internal ID15454050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108181896..108346655hg38UCSC Ensembl
Innerchr1:108724518..108889277hg19UCSC Ensembl
Innerchr1:108526041..108690800hg18UCSC Ensembl
Innerchr1:108436560..108601319hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38164760
hg19164760
hg18164760
hg17164760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703107
Samples
Known GenesNBPF4, SLC25A24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526757
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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