A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019345



Internal ID19108563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156467003..156553160hg38UCSC Ensembl
Innerchr4:157388155..157474312hg19UCSC Ensembl
Innerchr4:157607605..157693762hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3886158
hg1986158
hg1886158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5445n100
Supporting Variantsnssv3636141
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)nsv1019345
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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