A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962746



Internal ID22737681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96787525..96787525hg38UCSC Ensembl
chr8:97799753..97799753hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430239
Samples
Known GenesCPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962746
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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