A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027820



Internal ID19117038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176621691..176666743hg38UCSC Ensembl
Innerchr4:177542842..177587894hg19UCSC Ensembl
Innerchr4:177779836..177824888hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3845053
hg1945053
hg1845053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635461
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)nsv1027820
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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