A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496989



Internal ID22554923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161244889..161250965hg38UCSC Ensembl
chr5:160671896..160677972hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg386077
hg196077
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841541
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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