A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962455



Internal ID22737390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36645303..36645303hg38UCSC Ensembl
chr9:36645300..36645300hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445215
Samples
Known GenesMELK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962455
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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