A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400904



Internal ID22458774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41685538..41685618hg38UCSC Ensembl
chr22:42081542..42081622hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962310
Supporting Variants
Samples
Known GenesNHP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400904
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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