A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607889



Internal ID6994820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1244346..1282278hg38UCSC Ensembl
Innerchr6:1244357..1282268hg38UCSC Ensembl
Outerchr6:1244336..1282289hg38UCSC Ensembl
chr6:1244581..1282513hg19UCSC Ensembl
Innerchr6:1244592..1282503hg19UCSC Ensembl
Outerchr6:1244571..1282524hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3837933
hg1937933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12174447
SamplesHG03624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607889
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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