A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635549



Internal ID18933830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177824913..177953102hg38UCSC Ensembl
Innerchr4:178746067..178874256hg19UCSC Ensembl
Innerchr4:178983061..179111250hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38128190
hg19128190
hg18128190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028173
Supporting Variants
Samples
Known GenesLINC01098, LINC01099
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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