A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415503



Internal ID22473373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170026312..170026380hg38UCSC Ensembl
chr4:170947463..170947531hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415503
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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