A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373847



Internal ID22599516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47850460..47850597hg38UCSC Ensembl
chr16:47884371..47884508hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373847
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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