A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332271



Internal ID20865441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:68105405..68108678hg38UCSC Ensembl
chr1:68571088..68574361hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383274
hg193274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062710
Samples
Known GenesGNG12-AS1, WLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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