A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448665



Internal ID21106218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84137080..84144555hg38UCSC Ensembl
chr10:85896836..85904311hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg387476
hg197476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984584
Samples
Known GenesGHITM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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