A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372991



Internal ID22598660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77317997..77318092hg38UCSC Ensembl
chr13:77892132..77892227hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943042
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372991
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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