A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381822



Internal ID21039375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25865501..25870600hg38UCSC Ensembl
chr5:25865610..25870709hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5704n223
Supporting Variantsnssv18131173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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