A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576668



Internal ID21768711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157611706..157611762hg38UCSC Ensembl
chr7:157404398..157404454hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009269
Supporting Variants
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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