A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14890297



Internal ID5619354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106381096..106386345hg38UCSC Ensembl
Innerchr13:106381123..106386318hg38UCSC Ensembl
Outerchr13:106381069..106386372hg38UCSC Ensembl
chr13:107033444..107038693hg19UCSC Ensembl
Innerchr13:107033471..107038666hg19UCSC Ensembl
Outerchr13:107033417..107038720hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385250
hg195250
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633465
Supporting Variants
SamplesNA19043
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14890297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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