A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978250



Internal ID20545290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116351548..116352280hg38UCSC Ensembl
chr10:118111060..118111792hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449144
Supporting Variants
Samples
Known GenesCCDC172
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00071


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