A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023600



Internal ID19112817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17382495..17418221hg38UCSC Ensembl
Innerchr5:17382604..17418330hg19UCSC Ensembl
Innerchr5:17435604..17471330hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3835727
hg1935727
hg1835727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5578n100
Supporting Variantsnssv3638309
Samples
Known GenesLOC401177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023600
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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