A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754616



Internal ID21389663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18401860..18402636hg38UCSC Ensembl
chr6:18402091..18402867hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434881
Supporting Variants
SamplesNB10
Known GenesRNF144B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754616
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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