A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015551



Internal ID19104768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161272388..161283947hg38UCSC Ensembl
Innerchr4:162193540..162205099hg19UCSC Ensembl
Innerchr4:162412990..162424549hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3811560
hg1911560
hg1811560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634143
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)nsv1015551
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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