A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407268



Internal ID22465138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119936323..119938012hg38UCSC Ensembl
chr3:119655170..119656859hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896101
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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