A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027946



Internal ID19117164
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 StatusM
Merged Variantsdgv5391n100
Supporting Variantsnssv3639492
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)nsv1027946
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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