A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381904



Internal ID22439774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20900729..20990968hg38UCSC Ensembl
chr17:20804042..20894281hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3890240
hg1990240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943717
Supporting Variants
Samples
Known GenesLOC440416
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381904
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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