A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860136



Internal ID22635071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33624595..33626747hg38UCSC Ensembl
chr9:33624593..33626745hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382153
hg192153
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512974
Samples
Known GenesANXA2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860136
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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