A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611299



Internal ID6998208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153519180..153534911hg38UCSC Ensembl
Innerchr6:153519180..153534911hg38UCSC Ensembl
Outerchr6:153518680..153535411hg38UCSC Ensembl
chr6:153840315..153856046hg19UCSC Ensembl
Innerchr6:153840315..153856046hg19UCSC Ensembl
Outerchr6:153839815..153856546hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3815732
hg1915732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12590716, essv12590715
SamplesNA21110, NA21090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611299
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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