A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525495



Internal ID15452788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60654096..60655651hg38UCSC Ensembl
Innerchr8:61566655..61568210hg19UCSC Ensembl
Innerchr8:61729209..61730764hg18UCSC Ensembl
Innerchr8:61729209..61730764hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381556
hg191556
hg181556
hg171556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701627
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525495
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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