A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569632



Internal ID21761675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105152217..105152275hg38UCSC Ensembl
chr7:104792664..104792722hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002898
Supporting Variants
Samples
Known GenesSRPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569632
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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