A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528524



Internal ID15109131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37789148..37839356hg38UCSC Ensembl
Innerchr8:37646666..37696874hg19UCSC Ensembl
Innerchr8:37765824..37816032hg18UCSC Ensembl
Innerchr8:37765824..37816032hg17UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3850209
hg1950209
hg1850209
hg1750209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705134
Samples
Known GenesGPR124
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528524
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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