A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570773



Internal ID21762816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51203205..51203477hg38UCSC Ensembl
chr7:51270902..51271174hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002631
Supporting Variants
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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