A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033839



Internal ID19123060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185945915..186005089hg38UCSC Ensembl
Innerchr4:186867069..186926243hg19UCSC Ensembl
Innerchr4:187104063..187163237hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3859175
hg1959175
hg1859175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635629
Samples
Known GenesSORBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033839
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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