A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961762



Internal ID22736704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14140508..14140508hg38UCSC Ensembl
chr6:14140739..14140739hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961762
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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