A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845729



Internal ID22620664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8180126..8181225hg38UCSC Ensembl
chr6:8180359..8181458hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508418, nssv17508417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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