A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12581197



Internal ID3709662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150106346..150114561hg38UCSC Ensembl
Innerchr6:150106846..150114061hg38UCSC Ensembl
Outerchr6:150105346..150115561hg38UCSC Ensembl
chr6:150427482..150435697hg19UCSC Ensembl
Innerchr6:150427982..150435197hg19UCSC Ensembl
Outerchr6:150426482..150436697hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388216
hg198216
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611226
Supporting Variants
SamplesHG03311
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12581197
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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