A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890763



Internal ID18838379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:162002676..162027451hg38UCSC Ensembl
Outerchr5:162002676..162027452hg38UCSC Ensembl
Innerchr5:161429682..161454457hg19UCSC Ensembl
Outerchr5:161429682..161454458hg19UCSC Ensembl
Innerchr5:161362260..161387035hg18UCSC Ensembl
Outerchr5:161362260..161387036hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3824777
hg1924777
hg1824777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799889, essv25781153, essv25784946, essv25796762, essv25797535
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890763
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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