A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610358



Internal ID6997275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110344667..110348688hg38UCSC Ensembl
Innerchr6:110344680..110348676hg38UCSC Ensembl
Outerchr6:110344655..110348701hg38UCSC Ensembl
chr6:110665870..110669891hg19UCSC Ensembl
Innerchr6:110665883..110669879hg19UCSC Ensembl
Outerchr6:110665858..110669904hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384022
hg194022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1210e214
Supporting Variantsessv12502093
SamplesHG00632
Known GenesMETTL24
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610358
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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