A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204376



Internal ID22353233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154687105..154687220hg38UCSC Ensembl
chr6:155008239..155008354hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331502
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204376
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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