A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451805



Internal ID21109358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71903077..71906769hg38UCSC Ensembl
chr10:73662835..73666527hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383693
hg193693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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