A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602663



Internal ID6642919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150789999..150798087hg38UCSC Ensembl
Innerchr4:150790008..150798078hg38UCSC Ensembl
Outerchr4:150789990..150798096hg38UCSC Ensembl
chr4:151711151..151719239hg19UCSC Ensembl
Innerchr4:151711160..151719230hg19UCSC Ensembl
Outerchr4:151711142..151719248hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg388089
hg198089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11653092
SamplesHG03391
Known GenesLRBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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