A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11166369



Internal ID6026775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144381983..144399196hg38UCSC Ensembl
Innerchr3:144382133..144399046hg38UCSC Ensembl
Outerchr3:144381833..144399346hg38UCSC Ensembl
chr3:144100825..144118038hg19UCSC Ensembl
Innerchr3:144100975..144117888hg19UCSC Ensembl
Outerchr3:144100675..144118188hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3817214
hg1917214
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598035
Supporting Variants
SamplesNA19436
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11166369
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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