A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846081



Internal ID22621016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73611117..73612316hg38UCSC Ensembl
chr6:74320840..74322039hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507974
Samples
Known GenesSLC17A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846081
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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