A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611443



Internal ID6651662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160726265..160726890hg38UCSC Ensembl
Innerchr6:160726281..160726874hg38UCSC Ensembl
Outerchr6:160726249..160726906hg38UCSC Ensembl
chr6:161147297..161147922hg19UCSC Ensembl
Innerchr6:161147313..161147906hg19UCSC Ensembl
Outerchr6:161147281..161147938hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12612288, essv12612289, essv12612290, essv12612287
SamplesHG02025, HG01815, HG00599, HG00704
Known GenesPLG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611443
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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