A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181013



Internal ID21319809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93785720..93786713hg38UCSC Ensembl
chr10:95545477..95546470hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952506
Supporting Variants
SamplesHG002
Known GenesLGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181013
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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