A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568288



Internal ID21760331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45084230..45084347hg38UCSC Ensembl
chr7:45123829..45123946hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005806
Supporting Variants
Samples
Known GenesNACAD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568288
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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