A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441436



Internal ID21098989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14306956..14311973hg38UCSC Ensembl
chr11:14328502..14333519hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385018
hg195018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988317
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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