A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110917



Internal ID20677957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153786689..153788243hg38UCSC Ensembl
chr4:154707841..154709395hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381555
hg191555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393367
Supporting Variants
Samples
Known GenesSFRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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