A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12461654



Internal ID1847977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91088970..91090840hg38UCSC Ensembl
Innerchr6:91088998..91090812hg38UCSC Ensembl
Outerchr6:91088942..91090868hg38UCSC Ensembl
chr6:91798688..91800558hg19UCSC Ensembl
Innerchr6:91798716..91800530hg19UCSC Ensembl
Outerchr6:91798660..91800586hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381871
hg191871
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609932
Supporting Variants
SamplesHG01710
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12461654
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer