A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478758



Internal ID22536660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56223604..56224603hg38UCSC Ensembl
chr19:56734973..56735972hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872532
Supporting Variants
Samples
Known GenesZSCAN5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478758
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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