A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900903



Internal ID22676050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57598919..57598973hg38UCSC Ensembl
chr5:56894746..56894800hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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