A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608805



Internal ID6995729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42829564..42836399hg38UCSC Ensembl
Innerchr6:42829564..42836399hg38UCSC Ensembl
Outerchr6:42829064..42836899hg38UCSC Ensembl
chr6:42797302..42804137hg19UCSC Ensembl
Innerchr6:42797302..42804137hg19UCSC Ensembl
Outerchr6:42796802..42804637hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg386836
hg196836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12329135
SamplesNA18548
Known GenesGLTSCR1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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