A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611250



Internal ID6998160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151156413..151160220hg38UCSC Ensembl
Innerchr6:151156463..151160170hg38UCSC Ensembl
Outerchr6:151156363..151160270hg38UCSC Ensembl
chr6:151477548..151481355hg19UCSC Ensembl
Innerchr6:151477598..151481305hg19UCSC Ensembl
Outerchr6:151477498..151481405hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383808
hg193808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12581418
SamplesHG00379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611250
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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