A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031060



Internal ID19120281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131487874..131539214hg38UCSC Ensembl
Innerchr4:132409029..132460369hg19UCSC Ensembl
Innerchr4:132628479..132679819hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3851341
hg1951341
hg1851341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5389n100
Supporting Variantsnssv3639479, nssv3639478
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)nsv1031060
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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