A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853176



Internal ID22628111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133700612..133718688hg38UCSC Ensembl
chr9:136565734..136583810hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3818077
hg1918077
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511695
Samples
Known GenesSARDH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853176
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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