A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432702



Internal ID21090255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61351251..61351652hg38UCSC Ensembl
chr8:62263810..62264211hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168724
Samples
Known GenesCLVS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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