A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400128



Internal ID21057681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106892416..106932333hg38UCSC Ensembl
chr5:106228117..106268034hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3839918
hg1939918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5879n223
Supporting Variantsnssv18124153
Samples
Known GenesLOC102467213
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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