A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890192



Internal ID3892008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88555882..88703649hg38UCSC Ensembl
chr10:90315639..90463406hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38147768
hg19147768
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624134
Supporting Variants
SamplesHG02309
Known GenesLIPF, LIPJ, RNLS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890192
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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