A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947854



Internal ID22723346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44992613..44992613hg38UCSC Ensembl
chr7:45032212..45032212hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947854
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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