A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017572



Internal ID20584612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29531428..29531836hg38UCSC Ensembl
chr14:30000634..30001042hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490543
Supporting Variants
Samples
Known GenesMIR548AI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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