A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141760



Internal ID20708800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36526973..36538028hg38UCSC Ensembl
chr6:36494750..36505805hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3811056
hg1911056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413172
Supporting Variants
Samples
Known GenesSTK38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer