A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009464



Internal ID19098682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:27942348..27991227hg38UCSC Ensembl
Innerchr4:27943970..27992849hg19UCSC Ensembl
Innerchr4:27553068..27601947hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3848880
hg1948880
hg1848880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620618
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)nsv1009464
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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