A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12199816



Internal ID3001021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15040603..15049953hg38UCSC Ensembl
Innerchr6:15040619..15049937hg38UCSC Ensembl
Outerchr6:15040587..15049969hg38UCSC Ensembl
chr6:15040834..15050184hg19UCSC Ensembl
Innerchr6:15040850..15050168hg19UCSC Ensembl
Outerchr6:15040818..15050200hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg389351
hg199351
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608159
Supporting Variants
SamplesHG02648
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12199816
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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