A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896552



Internal ID22671646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148362931..148370374hg38UCSC Ensembl
chr5:147742494..147749937hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg387444
hg197444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419333
Samples
Known GenesLOC102546294
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896552
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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