A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845261



Internal ID22620196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36564939..36567164hg38UCSC Ensembl
chr6:36532716..36534941hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382226
hg192226
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845261
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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