A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892948



Internal ID22668004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63643600..63684630hg38UCSC Ensembl
chr5:62939427..62980457hg19UCSC Ensembl
Cytoband5q12.2
Allele length
AssemblyAllele length
hg3841031
hg1941031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892948
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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