A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596900



Internal ID6984214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87820260..87823510hg38UCSC Ensembl
Innerchr3:87820260..87823510hg38UCSC Ensembl
Outerchr3:87820177..87823539hg38UCSC Ensembl
chr3:87869410..87872660hg19UCSC Ensembl
Innerchr3:87869410..87872660hg19UCSC Ensembl
Outerchr3:87869327..87872689hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg383251
hg193251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11066128, essv11066123, essv11066122, essv11066119, essv11066127, essv11066125, essv11066126, essv11066121, essv11066118, essv11066120, essv11066124
SamplesHG00457, HG02185, HG00458, HG03624, HG00419, HG02070, HG02142, HG01845, HG00607, HG02079, HG00593
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596900
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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