A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844332



Internal ID22619267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118787325..118791938hg38UCSC Ensembl
chr6:119108488..119113101hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384614
hg194614
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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