A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360549



Internal ID21018102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81705389..81711588hg38UCSC Ensembl
chr3:81754540..81760739hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103175
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360549
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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