A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401055



Internal ID21058608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112831260..112834354hg38UCSC Ensembl
chr5:112166957..112170051hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg383095
hg193095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123104
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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