A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605495



Internal ID6972425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77733774..77744235hg38UCSC Ensembl
Innerchr5:77733783..77744227hg38UCSC Ensembl
Outerchr5:77733766..77744244hg38UCSC Ensembl
chr5:77029599..77040059hg19UCSC Ensembl
Innerchr5:77029608..77040051hg19UCSC Ensembl
Outerchr5:77029591..77040068hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3810462
hg1910461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11949212
SamplesNA20868
Known GenesTBCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605495
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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