A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373206



Internal ID22598875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77286909..77287684hg38UCSC Ensembl
chr13:77861044..77861819hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929280
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373206
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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