A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611309



Internal ID6998218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153920580..153963622hg38UCSC Ensembl
Innerchr6:153920599..153963604hg38UCSC Ensembl
Outerchr6:153920562..153963641hg38UCSC Ensembl
chr6:154241715..154284757hg19UCSC Ensembl
Innerchr6:154241734..154284739hg19UCSC Ensembl
Outerchr6:154241697..154284776hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3843043
hg1943043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12592323
SamplesHG01464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611309
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