A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462238



Internal ID21119791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84663295..85663452hg38UCSC Ensembl
chr11:84374338..85374496hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381000158
hg191000159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178000
Samples
Known GenesCREBZF, DLG2, TMEM126A, TMEM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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