A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3549626



Internal ID22418569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9221418..9221418hg38UCSC Ensembl
chr12:9374014..9374014hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386876, nssv14441767
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3549626
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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