A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710342



Internal ID134008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2832381..2850494hg38UCSC Ensembl
chr17:2735675..2753788hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3818114
hg1918114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530235
Supporting Variants
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710342
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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