A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14440749



Internal ID22237235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132192012..132192066hg38UCSC Ensembl
chr10:134005516..134005570hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190618
Supporting Variants
SamplesHG00733
Known GenesDPYSL4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14440749
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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