A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387379



Internal ID22445249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87197898..87634772hg38UCSC Ensembl
chr13:87850153..88287027hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38436875
hg19436875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945419
Supporting Variants
Samples
Known GenesMIR4500, MIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387379
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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