A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844569



Internal ID22619504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2310663..2317965hg38UCSC Ensembl
chr6:2310897..2318199hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387303
hg197303
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504334
Samples
Known GenesGMDS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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