A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611402



Internal ID6998311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158731201..158736275hg38UCSC Ensembl
Innerchr6:158731351..158736125hg38UCSC Ensembl
Outerchr6:158731051..158736425hg38UCSC Ensembl
chr6:159152233..159157307hg19UCSC Ensembl
Innerchr6:159152383..159157157hg19UCSC Ensembl
Outerchr6:159152083..159157457hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385075
hg195075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12605652
SamplesHG02757
Known GenesSYTL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611402
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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