A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849344



Internal ID22624279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71953409..71958108hg38UCSC Ensembl
chr9:74568325..74573024hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514219
Samples
Known GenesC9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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