A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601837



Internal ID6642092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114613329..114614873hg38UCSC Ensembl
Innerchr4:114613346..114614857hg38UCSC Ensembl
Outerchr4:114613313..114614890hg38UCSC Ensembl
chr4:115534485..115536029hg19UCSC Ensembl
Innerchr4:115534502..115536013hg19UCSC Ensembl
Outerchr4:115534469..115536046hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381545
hg191545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11572876
SamplesHG02180
Known GenesUGT8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601837
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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