A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023974



Internal ID21933317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43011311..43012392hg38UCSC Ensembl
chr17:41163328..41164409hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622947
Samples
Known GenesIFI35
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023974
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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