A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576972



Internal ID21769015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:206688..206739hg38UCSC Ensembl
chr7:206688..206739hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010864
Supporting Variants
Samples
Known GenesFAM20C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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