A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589768



Internal ID16377177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13831954..13865341hg38UCSC Ensembl
Innerchr3:13873451..13906838hg19UCSC Ensembl
Innerchr3:13848452..13881839hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3833388
hg1933388
hg1833388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959437
Samples
Known GenesWNT7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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