A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262400



Internal ID20471618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94950281..94950595hg38UCSC Ensembl
chr12:95344057..95344371hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745199
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262400
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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