A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12460057



Internal ID3889010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90282284..90293936hg38UCSC Ensembl
Innerchr6:90282284..90293936hg38UCSC Ensembl
Outerchr6:90281784..90294436hg38UCSC Ensembl
chr6:90992003..91003655hg19UCSC Ensembl
Innerchr6:90992003..91003655hg19UCSC Ensembl
Outerchr6:90991503..91004155hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3811653
hg1911653
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609919
Supporting Variants
SamplesHG03539
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12460057
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