A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960887



Internal ID22735847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170568765..170568765hg38UCSC Ensembl
chr6:170877853..170877853hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422871
Samples
Known GenesTBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960887
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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