A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602661



Internal ID6642917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150736590..150739044hg38UCSC Ensembl
Innerchr4:150736619..150739016hg38UCSC Ensembl
Outerchr4:150736562..150739073hg38UCSC Ensembl
chr4:151657742..151660196hg19UCSC Ensembl
Innerchr4:151657771..151660168hg19UCSC Ensembl
Outerchr4:151657714..151660225hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11653089
SamplesHG02657
Known GenesLRBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602661
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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