A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979176



Internal ID20546216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31334862..31335320hg38UCSC Ensembl
chr10:31623791..31624249hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448444
Supporting Variants
Samples
Known GenesZEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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