A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14446678



Internal ID22242371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42656067..42656160hg38UCSC Ensembl
chr18:40236032..40236125hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204124
Supporting Variants
SamplesHG00733
Known GenesLINC00907
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14446678
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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