A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889525



Internal ID22664544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9521137..9522309hg38UCSC Ensembl
chr5:9521249..9522421hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421777
Samples
Known GenesSEMA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889525
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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