A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401611



Internal ID21059164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72872853..72873345hg38UCSC Ensembl
chr5:72168680..72169172hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132174
Samples
Known GenesTNPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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