A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635598



Internal ID18933879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180403065..180505206hg38UCSC Ensembl
Innerchr4:181324218..181426359hg19UCSC Ensembl
Innerchr4:181561212..181663353hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38102142
hg19102142
hg18102142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028271
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)nssv3635598
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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