A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477312



Internal ID22535213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48641210..48643647hg38UCSC Ensembl
chr19:49144467..49146904hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871482
Supporting Variants
Samples
Known GenesCA11, SEC1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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