A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498414



Internal ID22556349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178707688..178715484hg38UCSC Ensembl
chr5:178134689..178142485hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387797
hg197797
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842229
Supporting Variants
Samples
Known GenesZNF354A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498414
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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