A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14449429



Internal ID22244739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71795379..71796794hg38UCSC Ensembl
chr12:72189159..72190574hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204808
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)nssv14449429
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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