A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639427



Internal ID18937708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127473502..127585807hg38UCSC Ensembl
Innerchr4:128394657..128506962hg19UCSC Ensembl
Innerchr4:128614107..128726412hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38112306
hg19112306
hg18112306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015564
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)nssv3639427
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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