A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605695



Internal ID6992633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85856134..85867040hg38UCSC Ensembl
Innerchr5:85856634..85866540hg38UCSC Ensembl
Outerchr5:85855134..85868040hg38UCSC Ensembl
chr5:85151952..85162858hg19UCSC Ensembl
Innerchr5:85152452..85162358hg19UCSC Ensembl
Outerchr5:85150952..85163858hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3810907
hg1910907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11964906
SamplesNA18504
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605695
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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