A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352909



Internal ID22318460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99535434..99535528hg38UCSC Ensembl
chr10:101295191..101295285hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527925
Supporting Variants
SamplesNA19240
Known GenesNKX2-3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352909
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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