A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611593



Internal ID6998499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164324976..164340961hg38UCSC Ensembl
Innerchr6:164324993..164340945hg38UCSC Ensembl
Outerchr6:164324960..164340978hg38UCSC Ensembl
chr6:164746009..164761994hg19UCSC Ensembl
Innerchr6:164746026..164761978hg19UCSC Ensembl
Outerchr6:164745993..164762011hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3815986
hg1915986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12626182, essv12626183, essv12626184
SamplesHG00187, NA19089, HG02464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611593
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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