A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116399



Internal ID20683439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42166717..42174156hg38UCSC Ensembl
chr4:42168734..42176173hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg387440
hg197440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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