A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529787



Internal ID22399178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15188177..15190593hg38UCSC Ensembl
chr6:15188408..15190824hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382417
hg192417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327531, nssv14327530, nssv14327529, nssv14327532, nssv14327528, nssv14327527
SamplesHG00512, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529787
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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