A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385916



Internal ID22443786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99548371..99561933hg38UCSC Ensembl
chr14:100014708..100028270hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3813563
hg1913563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939230
Supporting Variants
Samples
Known GenesCCDC85C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385916
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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