A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599971



Internal ID6987015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25615635..25620077hg38UCSC Ensembl
Innerchr4:25615652..25620061hg38UCSC Ensembl
Outerchr4:25615619..25620094hg38UCSC Ensembl
chr4:25617257..25621699hg19UCSC Ensembl
Innerchr4:25617274..25621683hg19UCSC Ensembl
Outerchr4:25617241..25621716hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11373390, essv11373391
SamplesHG01049, HG01197
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599971
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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