A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857523



Internal ID22632458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88443366..88452442hg38UCSC Ensembl
chr9:91058281..91067357hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389077
hg199077
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2160n209
Supporting Variantsnssv17514692
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857523
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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