A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13971710



Internal ID5607506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128458101..128463984hg38UCSC Ensembl
Innerchr10:128458103..128463983hg38UCSC Ensembl
Outerchr10:128458100..128463986hg38UCSC Ensembl
chr10:130256365..130262248hg19UCSC Ensembl
Innerchr10:130256367..130262247hg19UCSC Ensembl
Outerchr10:130256364..130262250hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg385884
hg195884
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624903
Supporting Variants
SamplesNA19037
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13971710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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