A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611254



Internal ID6651473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151190896..151201921hg38UCSC Ensembl
Innerchr6:151190908..151201910hg38UCSC Ensembl
Outerchr6:151190885..151201933hg38UCSC Ensembl
chr6:151512031..151523056hg19UCSC Ensembl
Innerchr6:151512043..151523045hg19UCSC Ensembl
Outerchr6:151512020..151523068hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3811026
hg1911026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12583019, essv12583017, essv12583021, essv12583020, essv12583018, essv12583022
SamplesNA20877, HG03968, NA20845, HG03697, HG02681, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611254
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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