A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134140



Internal ID20701180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81140104..81189611hg38UCSC Ensembl
chr5:80435923..80485430hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3849508
hg1949508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412261
Supporting Variants
Samples
Known GenesRASGRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134140
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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