A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10942959



Internal ID678251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19284011..19401107hg38UCSC Ensembl
Innerchr3:19284011..19401107hg38UCSC Ensembl
Outerchr3:19283511..19401607hg38UCSC Ensembl
chr3:19325503..19442599hg19UCSC Ensembl
Innerchr3:19325503..19442599hg19UCSC Ensembl
Outerchr3:19325003..19443099hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38117097
hg19117097
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595454
Supporting Variants
SamplesHG00319
Known GenesKCNH8, MIR4791
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10942959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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