A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845443



Internal ID22620378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75445701..75451050hg38UCSC Ensembl
chr6:76155417..76160766hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385350
hg195350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503109
Samples
Known GenesFILIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845443
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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