A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024978



Internal ID19114196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:92655332..92697978hg38UCSC Ensembl
Innerchr5:91991039..92033685hg19UCSC Ensembl
Innerchr5:92016795..92059441hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3842647
hg1942647
hg1842647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639192
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)nsv1024978
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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