A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456249



Internal ID22514126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96335501..96353194hg38UCSC Ensembl
chr11:96068665..96086358hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3817694
hg1917694
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850595
Supporting Variants
Samples
Known GenesCCDC82, MAML2, MIR1260B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456249
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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