A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595559



Internal ID21544165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11954073..11954143hg38UCSC Ensembl
chr17:11857390..11857460hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084518
SamplesHG00731
Known GenesDNAH9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595559
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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