A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529058



Internal ID22398451
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355639, nssv14355643, nssv14355640, nssv14355641, nssv14355642
SamplesNA19239, HG00732, NA19240, HG00733, HG00514
Known GenesLOC100188947
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529058
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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