A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844663



Internal ID22619598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151474375..151475895hg38UCSC Ensembl
chr6:151795510..151797030hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381521
hg191521
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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