A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032759



Internal ID19121981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2044003..2091517hg38UCSC Ensembl
Innerchr5:2044117..2091631hg19UCSC Ensembl
Innerchr5:2097117..2144631hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3847515
hg1947515
hg1847515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638515
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)nsv1032759
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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