A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025402



Internal ID21934745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74787297..74787398hg38UCSC Ensembl
chr17:72783436..72783537hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627402
Samples
Known GenesTMEM104
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025402
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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