A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515706



Internal ID15443317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126837454..126925273hg38UCSC Ensembl
Innerchr10:128526023..128613842hg19UCSC Ensembl
Innerchr10:128516013..128603832hg18UCSC Ensembl
Innerchr10:128516013..128603832hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3887820
hg1987820
hg1887820
hg1787820
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675205, nssv658963, nssv664497, nssv684791
Samples
Known GenesDOCK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515706
Frequency
Sample Size2026
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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