A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589767



Internal ID16030490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13802138..13881238hg38UCSC Ensembl
Innerchr3:13843635..13922735hg19UCSC Ensembl
Innerchr3:13818636..13897736hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3879101
hg1979101
hg1879101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959436
Samples
Known GenesWNT7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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