A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619744



Internal ID18918025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10689974..10706394hg38UCSC Ensembl
Innerchr4:10691598..10708018hg19UCSC Ensembl
Innerchr4:10300696..10317116hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3816421
hg1916421
hg1816421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012480
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)nssv3619744
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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