A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110161



Internal ID20677201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139045693..139046748hg38UCSC Ensembl
chr4:139966847..139967902hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390187
Supporting Variants
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110161
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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