A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14438869



Internal ID22235706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67650157..67650227hg38UCSC Ensembl
chr1:68115840..68115910hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177153
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14438869
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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