A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619251



Internal ID18917532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..51522hg38UCSC Ensembl
Innerchr4:12269..51416hg19UCSC Ensembl
Innerchr4:2269..41416hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839254
hg1939148
hg1839148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012666
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)nssv3619251
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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