A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897304



Internal ID22672405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75250003..75264973hg38UCSC Ensembl
chr5:74545828..74560798hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3814971
hg1914971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897304
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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