A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599900



Internal ID6986945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22406015..22407371hg38UCSC Ensembl
Innerchr4:22406017..22407370hg38UCSC Ensembl
Outerchr4:22406014..22407373hg38UCSC Ensembl
chr4:22407638..22408994hg19UCSC Ensembl
Innerchr4:22407640..22408993hg19UCSC Ensembl
Outerchr4:22407637..22408996hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370050
SamplesHG02419
Known GenesGPR125
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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