A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956510



Internal ID22709015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53192124..53192124hg38UCSC Ensembl
chr6:53056922..53056922hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956510
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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