A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461463



Internal ID22214047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35150828..35150893hg38UCSC Ensembl
chr10:35439756..35439821hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203434
Supporting Variants
SamplesHG00733
Known GenesCREM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14461463
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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