A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469801



Internal ID22527691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94309320..94319019hg38UCSC Ensembl
chr14:94775657..94785356hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861211
Supporting Variants
Samples
Known GenesSERPINA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469801
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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