A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292177



Internal ID20501395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112988860..112988970hg38UCSC Ensembl
chr13:113643174..113643284hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750058
Supporting Variants
Samples
Known GenesMCF2L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292177
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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