A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495645



Internal ID22553578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14274727..14276832hg38UCSC Ensembl
chr5:14274836..14276941hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841460
Supporting Variants
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495645
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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