A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291874



Internal ID20501092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96995992..96996100hg38UCSC Ensembl
chr7:96625304..96625412hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733976
Supporting Variants
Samples
Known GenesDLX6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291874
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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