A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436998



Internal ID21094551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3785042..3800716hg38UCSC Ensembl
chr11:3806272..3821946hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815675
hg1915675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190608
Samples
Known GenesNUP98, PGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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