A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636311



Internal ID21584616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16166956..16166956hg38UCSC Ensembl
chr5:16167065..16167065hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127290
SamplesHG02011
Known GenesMARCH11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636311
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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