A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388434



Internal ID22446304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58013236..58013415hg38UCSC Ensembl
chr17:56090597..56090776hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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