A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432800



Internal ID21090353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60360442..60360906hg38UCSC Ensembl
chr8:61273001..61273465hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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