A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586670



Internal ID21535225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71600639..71900634hg38UCSC Ensembl
chr11:71311685..71611680hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38299996
hg19299996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075972
SamplesNA20847
Known GenesALG1L9P, DEFB108B, FAM86C1, LOC100129216, LOC100133315, ZNF705E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586670
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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