A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530893



Internal ID306861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31876409..31876778hg38UCSC Ensembl
chr17:30203428..30203797hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712607
Samples
Known GenesUTP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530893
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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