A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456384



Internal ID22250643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39911775..39911775hg38UCSC Ensembl
chr6:39879519..39879519hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3533826
Supporting Variants
SamplesHG00733
Known GenesMOCS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456384
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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