A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020693



Internal ID19109912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61803038..62061205hg38UCSC Ensembl
Innerchr5:61098865..61357032hg19UCSC Ensembl
Innerchr5:61134622..61392789hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38258168
hg19258168
hg18258168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747226
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)nsv1020693
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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