A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639528



Internal ID18937809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132975997..133036084hg38UCSC Ensembl
Innerchr4:133897152..133957239hg19UCSC Ensembl
Innerchr4:134116602..134176689hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3860088
hg1960088
hg1860088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021604
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)nssv3639528
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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