A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611201



Internal ID6998112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148964888..148973111hg38UCSC Ensembl
Innerchr6:148964888..148973111hg38UCSC Ensembl
Outerchr6:148964388..148973611hg38UCSC Ensembl
chr6:149286024..149294247hg19UCSC Ensembl
Innerchr6:149286024..149294247hg19UCSC Ensembl
Outerchr6:149285524..149294747hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388224
hg198224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12580777
SamplesHG00250
Known GenesUST
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611201
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