A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597051



Internal ID6984365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95679383..95686013hg38UCSC Ensembl
Innerchr3:95679397..95685999hg38UCSC Ensembl
Outerchr3:95679369..95686027hg38UCSC Ensembl
chr3:95398227..95404857hg19UCSC Ensembl
Innerchr3:95398241..95404843hg19UCSC Ensembl
Outerchr3:95398213..95404871hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg386631
hg196631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11070352
SamplesHG01256
Known GenesMTHFD2P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597051
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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