A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527846



Internal ID22397233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87941590..87941662hg38UCSC Ensembl
chr6:88651308..88651380hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14329562, nssv14329560, nssv14329561, nssv14329563
SamplesNA19238, HG00731, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527846
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer