A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573643



Internal ID21765686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4778889..4778992hg38UCSC Ensembl
chr7:4818520..4818623hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012931
Supporting Variants
Samples
Known GenesAP5Z1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573643
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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