A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844308



Internal ID22619243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110862982..110864081hg38UCSC Ensembl
chr6:111184185..111185284hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501065, nssv17500924
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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