A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496352



Internal ID22554286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155107292..155122720hg38UCSC Ensembl
chr5:154486852..154502280hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3815429
hg1915429
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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