A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474652



Internal ID22532546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29484312..29485311hg38UCSC Ensembl
chr19:29975219..29976218hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869412
Supporting Variants
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474652
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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