A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956343



Internal ID22731535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77496260..77496260hg38UCSC Ensembl
chr7:77125577..77125577hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956343
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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