A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388825



Internal ID21046378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33044557..33045110hg38UCSC Ensembl
chr5:33044663..33045216hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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