A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439847



Internal ID21097400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27496901..27498300hg38UCSC Ensembl
chr11:27518448..27519847hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989815
Samples
Known GenesLIN7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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