A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11031499



Internal ID2357229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67771657..67772484hg38UCSC Ensembl
Innerchr3:67771667..67772474hg38UCSC Ensembl
Outerchr3:67771647..67772494hg38UCSC Ensembl
chr3:67822081..67822908hg19UCSC Ensembl
Innerchr3:67822091..67822898hg19UCSC Ensembl
Outerchr3:67822071..67822918hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596470
Supporting Variants
SamplesHG02087
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11031499
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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