A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024539



Internal ID19113756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6154192..6193139hg38UCSC Ensembl
Innerchr5:6154305..6193252hg19UCSC Ensembl
Innerchr5:6207305..6246252hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3838948
hg1938948
hg1838948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5558n100
Supporting Variantsnssv3746181
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)nsv1024539
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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