A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610903



Internal ID6997819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135951293..135964769hg38UCSC Ensembl
Innerchr6:135951343..135964719hg38UCSC Ensembl
Outerchr6:135951243..135964819hg38UCSC Ensembl
chr6:136272431..136285907hg19UCSC Ensembl
Innerchr6:136272481..136285857hg19UCSC Ensembl
Outerchr6:136272381..136285957hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3813477
hg1913477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12559855, essv12559854, essv12559853
SamplesNA19149, HG02095, NA19153
Known GenesPDE7B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610903
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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