A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027701



Internal ID19116920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116802590..116849890hg38UCSC Ensembl
Innerchr5:116138286..116185586hg19UCSC Ensembl
Innerchr5:116166185..116213485hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3847301
hg1947301
hg1847301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647213
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)nsv1027701
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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