A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356351



Internal ID22210140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95447297..95448263hg38UCSC Ensembl
chr10:97207054..97208020hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558444
Supporting Variants
SamplesHG00732
Known GenesSORBS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356351
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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