A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023723



Internal ID19112940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:4131644..4191462hg38UCSC Ensembl
Innerchr5:4131757..4191575hg19UCSC Ensembl
Innerchr5:4184757..4244575hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3859819
hg1959819
hg1859819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638525
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)nsv1023723
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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