A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037962



Internal ID21947305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75589376..75589431hg38UCSC Ensembl
chr17:73585457..73585512hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629541
Samples
Known GenesMYO15B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037962
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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