A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026528



Internal ID19115746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156481370..156583441hg38UCSC Ensembl
Innerchr4:157402522..157504593hg19UCSC Ensembl
Innerchr4:157621972..157724043hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38102072
hg19102072
hg18102072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5445n100
Supporting Variantsnssv3636142
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)nsv1026528
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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