A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599029



Internal ID6986077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188356895..188376313hg38UCSC Ensembl
Innerchr3:188357045..188376163hg38UCSC Ensembl
Outerchr3:188356745..188376463hg38UCSC Ensembl
chr3:188074683..188094101hg19UCSC Ensembl
Innerchr3:188074833..188093951hg19UCSC Ensembl
Outerchr3:188074533..188094251hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3819419
hg1919419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11264332, essv11264331, essv11264334, essv11264333
SamplesNA19917, HG00705, HG03061, HG00437
Known GenesLPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599029
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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