A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890517



Internal ID3892333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88813204..88815516hg38UCSC Ensembl
Innerchr10:88813226..88815495hg38UCSC Ensembl
Outerchr10:88813183..88815538hg38UCSC Ensembl
chr10:90572961..90575273hg19UCSC Ensembl
Innerchr10:90572983..90575252hg19UCSC Ensembl
Outerchr10:90572940..90575295hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382313
hg192313
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624142
Supporting Variants
SamplesHG03172
Known GenesLIPM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890517
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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