A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963528



Internal ID22738463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104195017..104195017hg38UCSC Ensembl
chr7:103835465..103835465hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442753
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963528
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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