A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265078



Internal ID20474296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121648763..121649496hg38UCSC Ensembl
chr7:121288817..121289550hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265078
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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