A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213308



Internal ID22360294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66469694..66469796hg38UCSC Ensembl
chr15:66762032..66762134hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387642
SamplesHG00512
Known GenesMAP2K1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213308
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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