A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524929



Internal ID301111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33437000..33443980hg38UCSC Ensembl
chr17:31764018..31770998hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386981
hg196981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712709
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524929
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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