A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369908



Internal ID22595577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65066859..65069085hg38UCSC Ensembl
chr14:65533577..65535803hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382227
hg192227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928624
Supporting Variants
Samples
Known GenesMAX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369908
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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