A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418777



Internal ID21076330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96238001..96241000hg38UCSC Ensembl
chr8:97250229..97253228hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173776
Samples
Known GenesMTERFD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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