A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357134



Internal ID22582803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12916330..12916517hg38UCSC Ensembl
chr10:12958330..12958517hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911984
Supporting Variants
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357134
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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