A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381893



Internal ID21039446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34835276..34839179hg38UCSC Ensembl
chr5:34835381..34839284hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg383904
hg193904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129741
Samples
Known GenesTTC23L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381893
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