A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595046



Internal ID6635321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2977948..2979659hg38UCSC Ensembl
Innerchr3:2977985..2979622hg38UCSC Ensembl
Outerchr3:2977911..2979696hg38UCSC Ensembl
chr3:3019632..3021343hg19UCSC Ensembl
Innerchr3:3019669..3021306hg19UCSC Ensembl
Outerchr3:3019595..3021380hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10901961
SamplesHG01866
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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