A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611329



Internal ID6998238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154759106..154760410hg38UCSC Ensembl
Innerchr6:154759112..154760405hg38UCSC Ensembl
Outerchr6:154759101..154760416hg38UCSC Ensembl
chr6:155080240..155081544hg19UCSC Ensembl
Innerchr6:155080246..155081539hg19UCSC Ensembl
Outerchr6:155080235..155081550hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381305
hg191305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12594533, essv12594534
SamplesHG04206, HG03951
Known GenesSCAF8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611329
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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