A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849840



Internal ID22624775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104131923..104134422hg38UCSC Ensembl
chr7:103772370..103774869hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503791
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849840
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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