A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968665



Internal ID22743600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7495078..7495078hg38UCSC Ensembl
chr19:7559964..7559964hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968665
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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