A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400647



Internal ID21058200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57369339..57378917hg38UCSC Ensembl
chr5:56665166..56674744hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg389579
hg199579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400647
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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