A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625051



Internal ID18923332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43186279..43214677hg38UCSC Ensembl
Innerchr4:43188296..43216694hg19UCSC Ensembl
Innerchr4:42883053..42911451hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3828399
hg1928399
hg1828399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998050
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)nssv3625051
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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