A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902011



Internal ID3141572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94162587..94165359hg38UCSC Ensembl
Innerchr10:94162637..94165309hg38UCSC Ensembl
Outerchr10:94162537..94165409hg38UCSC Ensembl
chr10:95922344..95925116hg19UCSC Ensembl
Innerchr10:95922394..95925066hg19UCSC Ensembl
Outerchr10:95922294..95925166hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382773
hg192773
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624247
Supporting Variants
SamplesHG02769
Known GenesPLCE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902011
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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