A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497652



Internal ID22555586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17015618..17022511hg38UCSC Ensembl
chr5:17015727..17022620hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386894
hg196894
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497652
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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