A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269647



Internal ID20478865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16197538..16198754hg38UCSC Ensembl
chr7:16237163..16238379hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742517
Supporting Variants
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269647
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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