A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12607887



Internal ID5435751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158891944..158893423hg38UCSC Ensembl
Innerchr6:158891958..158893410hg38UCSC Ensembl
Outerchr6:158891931..158893437hg38UCSC Ensembl
chr6:159312976..159314455hg19UCSC Ensembl
Innerchr6:159312990..159314442hg19UCSC Ensembl
Outerchr6:159312963..159314469hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611406
Supporting Variants
SamplesNA18959
Known GenesC6orf99
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12607887
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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