A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461104



Internal ID21118657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62209635..62237836hg38UCSC Ensembl
chr11:61977107..62005308hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3828202
hg1928202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196695
Samples
Known GenesSCGB2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461104
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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