A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711083



Internal ID134749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5868421..5886961hg38UCSC Ensembl
chr17:5771741..5790281hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3818541
hg1918541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145296
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711083
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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