A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386967



Internal ID22444837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28172152..28172296hg38UCSC Ensembl
chr17:26499178..26499322hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935094
Supporting Variants
Samples
Known GenesNLK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386967
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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