A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611106



Internal ID6998017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144326074..144333786hg38UCSC Ensembl
Innerchr6:144326107..144333754hg38UCSC Ensembl
Outerchr6:144326042..144333819hg38UCSC Ensembl
chr6:144647210..144654922hg19UCSC Ensembl
Innerchr6:144647243..144654890hg19UCSC Ensembl
Outerchr6:144647178..144654955hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387713
hg197713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12576157, essv12576159, essv12576156, essv12576158, essv12576155
SamplesNA20321, NA19027, HG03547, NA19042, NA20357
Known GenesUTRN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611106
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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