A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008508



Internal ID21917851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96147254..96147492hg38UCSC Ensembl
chr8:97159482..97159720hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577620
Samples
Known GenesGDF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008508
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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