A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724977



Internal ID148643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61914503..61915531hg38UCSC Ensembl
chr17:59991864..59992892hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532435
Supporting Variants
Samples
Known GenesINTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724977
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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