A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401906



Internal ID21059459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97718777..97908922hg38UCSC Ensembl
chr5:97054481..97244626hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38190146
hg19190146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5824n223
Supporting Variantsnssv18136197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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