A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611109



Internal ID6998020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144406981..144419415hg38UCSC Ensembl
Innerchr6:144407012..144419384hg38UCSC Ensembl
Outerchr6:144406950..144419446hg38UCSC Ensembl
chr6:144728117..144740551hg19UCSC Ensembl
Innerchr6:144728148..144740520hg19UCSC Ensembl
Outerchr6:144728086..144740582hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3812435
hg1912435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12576163
SamplesHG00173
Known GenesUTRN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611109
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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