A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527478



Internal ID15108085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26851469..26975681hg38UCSC Ensembl
Innerchr8:26708986..26833198hg19UCSC Ensembl
Innerchr8:26764903..26889115hg18UCSC Ensembl
Innerchr8:26764903..26889115hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38124213
hg19124213
hg18124213
hg17124213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703922
Samples
Known GenesADRA1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527478
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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