A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845634



Internal ID22620569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51339832..51342531hg38UCSC Ensembl
chr6:51204630..51207329hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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