A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472639



Internal ID22530531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10894716..10899463hg38UCSC Ensembl
chr19:11005392..11010139hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884383
Supporting Variants
Samples
Known GenesCARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472639
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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