A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001729



Internal ID19090946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14464618..14502056hg38UCSC Ensembl
Innerchr4:14466242..14503680hg19UCSC Ensembl
Innerchr4:14075340..14112778hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3837439
hg1937439
hg1837439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619839
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)nsv1001729
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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