A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432660



Internal ID21090213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29944613..29945245hg38UCSC Ensembl
chr8:29802129..29802761hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166831
Samples
Known GenesFAM183CP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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