A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497727



Internal ID22555661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174418572..174420552hg38UCSC Ensembl
chr5:173845575..173847555hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497727
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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