A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14875755



Internal ID4877571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100103635..100106765hg38UCSC Ensembl
Innerchr13:100103685..100106566hg38UCSC Ensembl
Outerchr13:100103546..100106854hg38UCSC Ensembl
chr13:100755889..100759019hg19UCSC Ensembl
Innerchr13:100755939..100758820hg19UCSC Ensembl
Outerchr13:100755800..100759108hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383131
hg193131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633340
Supporting Variants
SamplesHG03953
Known GenesPCCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14875755
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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