A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527887



Internal ID15455180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125636884..125696735hg38UCSC Ensembl
Innerchr10:127325453..127385304hg19UCSC Ensembl
Innerchr10:127315443..127375294hg18UCSC Ensembl
Innerchr10:127315443..127375294hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3859852
hg1959852
hg1859852
hg1759852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704390
Samples
Known GenesLOC283038, TEX36
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527887
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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