A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846064



Internal ID22620999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70264810..70276053hg38UCSC Ensembl
chr6:70974513..70985756hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811244
hg1911244
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507934
Samples
Known GenesCOL9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846064
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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