A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398708



Internal ID22456578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9791807..9792029hg38UCSC Ensembl
chr19:9902483..9902705hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398708
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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