A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599704



Internal ID6986749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13525117..13530769hg38UCSC Ensembl
Innerchr4:13525267..13530619hg38UCSC Ensembl
Outerchr4:13524967..13530919hg38UCSC Ensembl
chr4:13526741..13532393hg19UCSC Ensembl
Innerchr4:13526891..13532243hg19UCSC Ensembl
Outerchr4:13526591..13532543hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385653
hg195653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11359256
SamplesHG03397
Known GenesLINC01097
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599704
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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