A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018411



Internal ID19107628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3922155..3953484hg38UCSC Ensembl
Innerchr5:3922269..3953598hg19UCSC Ensembl
Innerchr5:3975269..4006598hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3831330
hg1931330
hg1831330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638524, nssv3638523
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)nsv1018411
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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