A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610862



Internal ID6997779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133707783..133715120hg38UCSC Ensembl
Innerchr6:133707783..133715120hg38UCSC Ensembl
Outerchr6:133707503..133715392hg38UCSC Ensembl
chr6:134028921..134036258hg19UCSC Ensembl
Innerchr6:134028921..134036258hg19UCSC Ensembl
Outerchr6:134028641..134036530hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387338
hg197338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220e214
Supporting Variantsessv12557513, essv12557514, essv12557512, essv12557511, essv12557510
SamplesHG02035, HG01842, HG01858, HG02371, HG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610862
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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