A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440256



Internal ID21097809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3002798..3004338hg38UCSC Ensembl
chr11:3024028..3025568hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990288
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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