A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381089



Internal ID22127290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66469896..66470118hg38UCSC Ensembl
chr15:66762234..66762456hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214476
Supporting Variants
SamplesHG00512
Known GenesMAP2K1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381089
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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