A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420283



Internal ID21077836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96136158..96225602hg38UCSC Ensembl
chr8:97148386..97237830hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3889445
hg1989445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228358
Samples
Known GenesGDF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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