A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524435



Internal ID15451728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11346844..11350668hg38UCSC Ensembl
Innerchr10:11388843..11392667hg19UCSC Ensembl
Innerchr10:11428849..11432673hg18UCSC Ensembl
Innerchr10:11428849..11432673hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383825
hg193825
hg183825
hg173825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700365
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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