A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12612287



Internal ID2614104
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611443
Supporting Variants
SamplesHG00599
Known GenesPLG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12612287
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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