A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522877



Internal ID15450170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125362698..125403852hg38UCSC Ensembl
Innerchr10:127051267..127092421hg19UCSC Ensembl
Innerchr10:127041257..127082411hg18UCSC Ensembl
Innerchr10:127041257..127082411hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3841155
hg1941155
hg1841155
hg1741155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698532
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522877
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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