A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978947



Internal ID20545987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17008128..17556465hg38UCSC Ensembl
chr10:17050127..17598464hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38548338
hg19548338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448356
Supporting Variants
Samples
Known GenesCUBN, ST8SIA6, ST8SIA6-AS1, TRDMT1, VIM, VIM-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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