A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12590716



Internal ID6903413
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611299
Supporting Variants
SamplesNA21110
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12590716
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer