A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115379



Internal ID20682419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169059134..169064156hg38UCSC Ensembl
chr4:169980285..169985307hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385023
hg195023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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