A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323998



Internal ID20857121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24067721..24069051hg38UCSC Ensembl
chr1:24394211..24395541hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060136
Samples
Known GenesMYOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323998
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