A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438994



Internal ID21096547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69583477..69609253hg38UCSC Ensembl
chr10:71343233..71369009hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3825777
hg1925777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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