A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464149



Internal ID21121702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62793354..62827923hg38UCSC Ensembl
chr11:62560826..62595395hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3834570
hg1934570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180185
Samples
Known GenesNXF1, STX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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