A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111537



Internal ID20678577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15473588..15474096hg38UCSC Ensembl
chr4:15475212..15475720hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373568
Supporting Variants
Samples
Known GenesCC2D2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00052


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