A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916241



Internal ID22691460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45258305..45259126hg38UCSC Ensembl
chr11:45279856..45280677hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369031
Samples
Known GenesSYT13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916241
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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