A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639492



Internal ID18937773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131591556..131631063hg38UCSC Ensembl
Innerchr4:132512711..132552218hg19UCSC Ensembl
Innerchr4:132732161..132771668hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3839508
hg1939508
hg1839508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027946
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)nssv3639492
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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