A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479187



Internal ID21136740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87518248..87563235hg38UCSC Ensembl
chr13:88170503..88215490hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3844988
hg1944988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014514
Samples
Known GenesMIR4500HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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