A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473212



Internal ID22531104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13815636..13817041hg38UCSC Ensembl
chr19:13926450..13927855hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873940
Supporting Variants
Samples
Known GenesZSWIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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