A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12457904



Internal ID2459720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89136169..89141974hg38UCSC Ensembl
Innerchr6:89136319..89141824hg38UCSC Ensembl
Outerchr6:89136019..89142124hg38UCSC Ensembl
chr6:89845888..89851693hg19UCSC Ensembl
Innerchr6:89846038..89851543hg19UCSC Ensembl
Outerchr6:89845738..89851843hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385806
hg195806
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609897
Supporting Variants
SamplesHG00500
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12457904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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