A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610291



Internal ID6997208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107077350..107080849hg38UCSC Ensembl
Innerchr6:107077371..107080828hg38UCSC Ensembl
Outerchr6:107077329..107080870hg38UCSC Ensembl
chr6:107398554..107402053hg19UCSC Ensembl
Innerchr6:107398575..107402032hg19UCSC Ensembl
Outerchr6:107398533..107402074hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499086
SamplesHG03563
Known GenesBEND3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610291
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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