A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700526



Internal ID15090492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236578945..236581261hg38UCSC Ensembl
Innerchr2:237487588..237489904hg19UCSC Ensembl
Innerchr2:237152327..237154643hg18UCSC Ensembl
Innerchr2:237269588..237271904hg17UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382317
hg192317
hg182317
hg172317
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524571
Supporting Variants
Samples
Known GenesACKR3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700526
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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