A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083794



Internal ID21435685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112988843..112988953hg38UCSC Ensembl
chr13:113643157..113643267hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585024
Supporting Variants
SamplesHG00731
Known GenesMCF2L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083794
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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