A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564844



Internal ID21889199
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 StatusS
Merged Variantsnsv6016441
Supporting Variants
Samples
Known GenesPSPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564844
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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