A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027711



Internal ID19116930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18608269..18662987hg38UCSC Ensembl
Innerchr5:18608378..18663096hg19UCSC Ensembl
Innerchr5:18644135..18698853hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3854719
hg1954719
hg1854719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5593n100
Supporting Variantsnssv3635887, nssv3635888
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)nsv1027711
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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