A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527929



Internal ID15455222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87900583..87954662hg38UCSC Ensembl
Innerchr3:87949733..88003812hg19UCSC Ensembl
Innerchr3:88032423..88086502hg18UCSC Ensembl
Innerchr3:88032423..88086502hg17UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3854080
hg1954080
hg1854080
hg1754080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704436
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527929
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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