A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890194



Internal ID3892010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88594312..88611587hg38UCSC Ensembl
Innerchr10:88594353..88611546hg38UCSC Ensembl
Outerchr10:88594271..88611628hg38UCSC Ensembl
chr10:90354069..90371344hg19UCSC Ensembl
Innerchr10:90354110..90371303hg19UCSC Ensembl
Outerchr10:90354028..90371385hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3817276
hg1917276
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624135
Supporting Variants
SamplesHG01848
Known GenesLIPJ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890194
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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