A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355643



Internal ID22292366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91577115..91577383hg38UCSC Ensembl
chr10:93336872..93337140hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529058
Supporting Variants
SamplesNA19240
Known GenesLOC100188947
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355643
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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