A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018077



Internal ID19107294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104174067..104209961hg38UCSC Ensembl
Innerchr5:103509768..103545662hg19UCSC Ensembl
Innerchr5:103537667..103573561hg18UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3835895
hg1935895
hg1835895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645970
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)nsv1018077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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