A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388180



Internal ID21045733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166827966..166828523hg38UCSC Ensembl
chr4:167749117..167749674hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112815
Samples
Known GenesSPOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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