A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114204



Internal ID20681244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176133661..176237419hg38UCSC Ensembl
chr4:177054812..177158570hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38103759
hg19103759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391322
Supporting Variants
Samples
Known GenesASB5, SPATA4, WDR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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