A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12461641



Internal ID2009399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90714133..90715436hg38UCSC Ensembl
Innerchr6:90714133..90715436hg38UCSC Ensembl
Outerchr6:90714044..90715516hg38UCSC Ensembl
chr6:91423852..91425155hg19UCSC Ensembl
Innerchr6:91423852..91425155hg19UCSC Ensembl
Outerchr6:91423763..91425235hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609928
Supporting Variants
SamplesHG01855
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12461641
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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