A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11094672



Internal ID1096488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106876525..106900950hg38UCSC Ensembl
Innerchr3:106876539..106900936hg38UCSC Ensembl
Outerchr3:106876511..106900964hg38UCSC Ensembl
chr3:106595372..106619797hg19UCSC Ensembl
Innerchr3:106595386..106619783hg19UCSC Ensembl
Outerchr3:106595358..106619811hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3824426
hg1924426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597294
Supporting Variants
SamplesNA19901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11094672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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