A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845515



Internal ID22620450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43149752..43150980hg38UCSC Ensembl
chr6:43117490..43118718hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1773n209
Supporting Variantsnssv17505800, nssv17505801
Samples
Known GenesPTK7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845515
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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