A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497191



Internal ID22555125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70692290..70699873hg38UCSC Ensembl
chr4:71558007..71565590hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg387584
hg197584
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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