A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641108



Internal ID18939389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135611369..135680874hg38UCSC Ensembl
Innerchr4:136532524..136602029hg19UCSC Ensembl
Innerchr4:136751974..136821479hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3869506
hg1969506
hg1869506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029055
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)nssv3641108
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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