A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560601



Internal ID21884956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107170717..107172247hg38UCSC Ensembl
chr7:106811162..106812692hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381531
hg191531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013804
Supporting Variants
Samples
Known GenesHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560601
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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