A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12457765



Internal ID2094643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89132295..89137224hg38UCSC Ensembl
Innerchr6:89132296..89137223hg38UCSC Ensembl
Outerchr6:89132294..89137225hg38UCSC Ensembl
chr6:89842014..89846943hg19UCSC Ensembl
Innerchr6:89842015..89846942hg19UCSC Ensembl
Outerchr6:89842013..89846944hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384930
hg194930
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609896
Supporting Variants
SamplesHG01896
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12457765
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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