A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527596



Internal ID15108203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:61647428..61733966hg38UCSC Ensembl
Innerchr10:63407186..63493724hg19UCSC Ensembl
Innerchr10:63077192..63163730hg18UCSC Ensembl
Innerchr10:63077192..63163730hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3886539
hg1986539
hg1886539
hg1786539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv42n21
Supporting Variantsnssv704057
Samples
Known GenesC10orf107
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527596
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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