A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595865



Internal ID6983183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36514234..36516004hg38UCSC Ensembl
Innerchr3:36514238..36516001hg38UCSC Ensembl
Outerchr3:36514231..36516008hg38UCSC Ensembl
chr3:36555726..36557496hg19UCSC Ensembl
Innerchr3:36555730..36557493hg19UCSC Ensembl
Outerchr3:36555723..36557500hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10980995
SamplesNA12400
Known GenesSTAC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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