A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374349



Internal ID22600018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10926352..10930083hg38UCSC Ensembl
chr17:10829669..10833400hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg383732
hg193732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374349
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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