A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335248



Internal ID20868440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214952110..214952707hg38UCSC Ensembl
chr1:215125453..215126050hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335248
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