A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038775



Internal ID21948118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45169926..45177104hg38UCSC Ensembl
chr17:43247293..43254471hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg387179
hg197179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624489
Samples
Known GenesHEXIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038775
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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