A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116100



Internal ID20683140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39557433..39558157hg38UCSC Ensembl
chr4:39559053..39559777hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394014
Supporting Variants
Samples
Known GenesMIR1273H, SMIM14, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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