A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441195



Internal ID21098748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101509271..101518077hg38UCSC Ensembl
chr10:103269028..103277834hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg388807
hg198807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977205
Samples
Known GenesBTRC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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