A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9899043



Internal ID6093621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34460494..34466933hg38UCSC Ensembl
Innerchr1:34460507..34466920hg38UCSC Ensembl
Outerchr1:34460481..34466946hg38UCSC Ensembl
chr1:34926095..34932534hg19UCSC Ensembl
Innerchr1:34926108..34932521hg19UCSC Ensembl
Outerchr1:34926082..34932547hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386440
hg196440
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585708
Supporting Variants
SamplesNA19473
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9899043
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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