A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037086



Internal ID21946429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81726027..81736578hg38UCSC Ensembl
chr17:79693057..79703608hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3810552
hg1910552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037086
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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