A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456910



Internal ID22251083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151450414..151450493hg38UCSC Ensembl
chr6:151771549..151771628hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3176541
Supporting Variants
SamplesHG00733
Known GenesRMND1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456910
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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