A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020435



Internal ID19109654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160445471..160581986hg38UCSC Ensembl
Innerchr4:161366623..161503138hg19UCSC Ensembl
Innerchr4:161586073..161722588hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38136516
hg19136516
hg18136516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633965
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)nsv1020435
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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