A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260331



Internal ID20469549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70481420..70481487hg38UCSC Ensembl
chr4:71347137..71347204hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746924
Supporting Variants
Samples
Known GenesMUC7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260331
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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