A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427601



Internal ID21085154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75208820..75210215hg38UCSC Ensembl
chr8:76121055..76122450hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381396
hg191396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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