A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016441



Internal ID21925784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56041365..56041476hg38UCSC Ensembl
chr7:56109058..56109169hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564844
Samples
Known GenesPSPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016441
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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