A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14392581



Internal ID22197383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90722031..90722401hg38UCSC Ensembl
chr15:91265262..91265632hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528779
Supporting Variants
SamplesHG00731
Known GenesBLM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14392581
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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