A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125825



Internal ID20692865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142102166..142252775hg38UCSC Ensembl
chr5:141481731..141632340hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38150610
hg19150610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401940
Supporting Variants
Samples
Known GenesNDFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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