A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382306



Internal ID22440176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35496102..35505224hg38UCSC Ensembl
chr17:33823121..33832243hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389123
hg199123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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