A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409145



Internal ID22467015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134179003..134179072hg38UCSC Ensembl
chr3:133897847..133897916hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899827
Supporting Variants
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409145
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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