A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119129



Internal ID20686169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70644381..70644760hg38UCSC Ensembl
chr4:71510098..71510477hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386940
Supporting Variants
Samples
Known GenesENAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00074


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