A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352933



Internal ID22194856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100001189..100001484hg38UCSC Ensembl
chr10:101760946..101761241hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527185
Supporting Variants
SamplesHG00731
Known GenesDNMBP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352933
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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