A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416997



Internal ID22474867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91323041..91421784hg38UCSC Ensembl
chr4:92244192..92342935hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3898744
hg1998744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892737
Supporting Variants
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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