A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845361



Internal ID22620296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71418981..71422138hg38UCSC Ensembl
chr6:72128684..72131841hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383158
hg193158
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507949
Samples
Known GenesLINC00472
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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