A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474695



Internal ID22532589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32769879..32773117hg38UCSC Ensembl
chr19:33260785..33264023hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383239
hg193239
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877179
Supporting Variants
Samples
Known GenesTDRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474695
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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