A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012692



Internal ID19101909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28120449..28163746hg38UCSC Ensembl
Innerchr4:28122071..28165368hg19UCSC Ensembl
Innerchr4:27731169..27774466hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3843298
hg1943298
hg1843298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5161n100
Supporting Variantsnssv3620622, nssv3620623
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012692
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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