A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017324



Internal ID20584364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36098494..36099708hg38UCSC Ensembl
chr14:36567700..36568914hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480863
Supporting Variants
Samples
Known GenesLINC00609
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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