A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12499270



Internal ID3105909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107960954..107975772hg38UCSC Ensembl
Innerchr6:107961104..107975622hg38UCSC Ensembl
Outerchr6:107960804..107975922hg38UCSC Ensembl
chr6:108282158..108296976hg19UCSC Ensembl
Innerchr6:108282308..108296826hg19UCSC Ensembl
Outerchr6:108282008..108297126hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3814819
hg1914819
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610306
Supporting Variants
SamplesHG02727
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12499270
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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