A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610880



Internal ID6997796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134482039..134484650hg38UCSC Ensembl
Innerchr6:134482050..134484640hg38UCSC Ensembl
Outerchr6:134482029..134484661hg38UCSC Ensembl
chr6:134803177..134805788hg19UCSC Ensembl
Innerchr6:134803188..134805778hg19UCSC Ensembl
Outerchr6:134803167..134805799hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg382612
hg192612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12559644, essv12559643
SamplesHG02058, HG01810
Known GenesLINC01010
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610880
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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