A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475962



Internal ID22533860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41749769..41787982hg38UCSC Ensembl
chr19:42253677..42291890hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3838214
hg1938214
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882322
Supporting Variants
Samples
Known GenesCEACAM6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475962
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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