A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636132



Internal ID18934413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155139619..155156105hg38UCSC Ensembl
Innerchr4:156060771..156077257hg19UCSC Ensembl
Innerchr4:156280221..156296707hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3816487
hg1916487
hg1816487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027434
Supporting Variants
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)nssv3636132
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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