A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528779



Internal ID22398171
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380604, nssv14374756, nssv14389020, nssv14373277, nssv14392581, nssv14377507, nssv14386265, nssv14375748, nssv14379134
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesBLM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528779
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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