A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464939



Internal ID21122492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61011889..61018693hg38UCSC Ensembl
chr11:60779361..60786165hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386805
hg196805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992674
Samples
Known GenesCD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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