A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027252



Internal ID21936595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74755729..74755951hg38UCSC Ensembl
chr17:72751868..72752090hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635119
Samples
Known GenesSLC9A3R1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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