A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601056



Internal ID6641314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76563547..76567859hg38UCSC Ensembl
Innerchr4:76563565..76567842hg38UCSC Ensembl
Outerchr4:76563530..76567877hg38UCSC Ensembl
chr4:77484700..77489012hg19UCSC Ensembl
Innerchr4:77484718..77488995hg19UCSC Ensembl
Outerchr4:77484683..77489030hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg384313
hg194313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11508293
SamplesNA19026
Known GenesSHROOM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601056
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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