A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597976



Internal ID6985113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141351206..141356749hg38UCSC Ensembl
Innerchr3:141351206..141356749hg38UCSC Ensembl
Outerchr3:141351077..141356857hg38UCSC Ensembl
chr3:141070048..141075591hg19UCSC Ensembl
Innerchr3:141070048..141075591hg19UCSC Ensembl
Outerchr3:141069919..141075699hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg385544
hg195544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11163840, essv11163838, essv11163839, essv11163837, essv11163836
SamplesHG02595, HG02461, HG02588, HG00734, NA21123
Known GenesZBTB38
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597976
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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