A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558363



Internal ID21882718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21227887..21227948hg38UCSC Ensembl
chr7:21267506..21267567hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558363
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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