A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036444



Internal ID21945787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46738928..46739057hg38UCSC Ensembl
chr17:44816294..44816423hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628700
Samples
Known GenesNSF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036444
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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