A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608158



Internal ID6995088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14970864..14976069hg38UCSC Ensembl
Innerchr6:14970887..14976047hg38UCSC Ensembl
Outerchr6:14970842..14976092hg38UCSC Ensembl
chr6:14971095..14976300hg19UCSC Ensembl
Innerchr6:14971118..14976278hg19UCSC Ensembl
Outerchr6:14971073..14976323hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385206
hg195206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12199815
SamplesNA19655
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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