A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597857



Internal ID6984995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134647587..134651285hg38UCSC Ensembl
Innerchr3:134647634..134651238hg38UCSC Ensembl
Outerchr3:134647540..134651332hg38UCSC Ensembl
chr3:134366429..134370127hg19UCSC Ensembl
Innerchr3:134366476..134370080hg19UCSC Ensembl
Outerchr3:134366382..134370174hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383699
hg193699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11156390
SamplesNA19982
Known GenesKY
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597857
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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