A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452001



Internal ID21109554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44978698..44986332hg38UCSC Ensembl
chr10:45474146..45481780hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387635
hg197635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980384
Samples
Known GenesC10orf10, RASSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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