A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391322



Internal ID21048875
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 StatusM
Merged Variants
Supporting Variantsnssv18114204
Samples
Known GenesASB5, SPATA4, WDR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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