A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383085



Internal ID22440955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47627187..47629131hg38UCSC Ensembl
chr17:45704553..45706497hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381945
hg191945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936605
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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