A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3556910



Internal ID22425724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62893487..62893487hg38UCSC Ensembl
chr15:63185686..63185686hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14444553
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)nsv3556910
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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