A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276011



Internal ID20485229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43834888..43834957hg38UCSC Ensembl
chr7:43874487..43874556hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276011
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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