A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334945



Internal ID20868135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19372843..19373770hg38UCSC Ensembl
chr1:19699337..19700264hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056222
Samples
Known GenesCAPZB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334945
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