A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031989



Internal ID19121211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97997587..98188649hg38UCSC Ensembl
Innerchr5:97333291..97524353hg19UCSC Ensembl
Innerchr5:97359047..97550109hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38191063
hg19191063
hg18191063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640466
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)nsv1031989
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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