A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524429



Internal ID15451722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141653549..141658488hg38UCSC Ensembl
Innerchr3:141372391..141377330hg19UCSC Ensembl
Innerchr3:142855081..142860020hg18UCSC Ensembl
Innerchr3:142855089..142860028hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg384940
hg194940
hg184940
hg174940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700356
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524429
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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