A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899687



Internal ID22674819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70587429..70598315hg38UCSC Ensembl
chr6:71297132..71308018hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3810887
hg1910887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441393
Samples
Known GenesC6orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899687
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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