A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600608



Internal ID6987650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57792014..57792903hg38UCSC Ensembl
Innerchr4:57792028..57792889hg38UCSC Ensembl
Outerchr4:57792000..57792917hg38UCSC Ensembl
chr4:58658180..58659069hg19UCSC Ensembl
Innerchr4:58658194..58659055hg19UCSC Ensembl
Outerchr4:58658166..58659083hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11443837
SamplesNA18633
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600608
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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