A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333646



Internal ID20866826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179151201..179152000hg38UCSC Ensembl
chr1:179120336..179121135hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054113
Samples
Known GenesABL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333646
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