A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205567



Internal ID22354243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2059176..2059708hg38UCSC Ensembl
chr6:2059410..2059942hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324804, nssv14324802, nssv14324803
SamplesNA19238, NA19239, NA19240
Known GenesGMDS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205567
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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