A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525654



Internal ID15452947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:61587284..61630160hg38UCSC Ensembl
Innerchr10:63347042..63389918hg19UCSC Ensembl
Innerchr10:63017048..63059924hg18UCSC Ensembl
Innerchr10:63017048..63059924hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3842877
hg1942877
hg1842877
hg1742877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701809
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525654
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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