A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18018031



Internal ID20585071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37401201..37402500hg38UCSC Ensembl
chr14:37870406..37871705hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479248
Supporting Variants
Samples
Known GenesMIPOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18018031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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