A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040371



Internal ID21949714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18201743..18201794hg38UCSC Ensembl
chr17:18105057..18105108hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632198
Samples
Known GenesALKBH5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040371
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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