A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600740



Internal ID6987780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:63473249..63522034hg38UCSC Ensembl
Innerchr4:63473749..63521534hg38UCSC Ensembl
Outerchr4:63472249..63523034hg38UCSC Ensembl
chr4:64338967..64387752hg19UCSC Ensembl
Innerchr4:64339467..64387252hg19UCSC Ensembl
Outerchr4:64337967..64388752hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3848786
hg1948786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11460623
SamplesNA20588
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600740
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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