A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849564



Internal ID22624499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94322720..94325019hg38UCSC Ensembl
chr14:94789057..94791356hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469802
Samples
Known GenesSERPINA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849564
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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