A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945419



Internal ID22720896
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 StatusM
Merged Variants
Supporting Variantsnssv17387379
Samples
Known GenesMIR4500, MIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945419
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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