A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527455



Internal ID22396841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155823005..155823178hg38UCSC Ensembl
chr6:156144139..156144312hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14329637, nssv14329639, nssv14329642, nssv14329640, nssv14329638, nssv14329641
SamplesHG00512, NA19238, NA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527455
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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