A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898247



Internal ID22673360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94068969..94069037hg38UCSC Ensembl
chr5:93404674..93404742hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423978
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898247
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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