A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441073



Internal ID21098626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3878089..3926396hg38UCSC Ensembl
chr11:3899319..3947626hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3848308
hg1948308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990714
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441073
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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