A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9896467



Internal ID6521760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32776270..32778868hg38UCSC Ensembl
Innerchr1:32776303..32778835hg38UCSC Ensembl
Outerchr1:32776237..32778901hg38UCSC Ensembl
chr1:33241871..33244469hg19UCSC Ensembl
Innerchr1:33241904..33244436hg19UCSC Ensembl
Outerchr1:33241838..33244502hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585677
Supporting Variants
SamplesHG04118
Known GenesYARS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9896467
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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