A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860976



Internal ID22635911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72139065..72140164hg38UCSC Ensembl
chr9:74753981..74755080hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514232, nssv17514233
Samples
Known GenesGDA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860976
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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