A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961842



Internal ID22736784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113105250..113105250hg38UCSC Ensembl
chr7:112745305..112745305hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961842
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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