A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116085



Internal ID20683125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39349781..39351021hg38UCSC Ensembl
chr4:39351401..39352641hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386345
Supporting Variants
Samples
Known GenesMIR1273H, RFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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