A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618267



Internal ID20991338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154948472..154969013hg38UCSC Ensembl
chr6:155269606..155290147hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3820542
hg1920542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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