A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432987



Internal ID21090540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65661801..65663100hg38UCSC Ensembl
chr8:66574036..66575335hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221542
Samples
Known GenesMTFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432987
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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