A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075265



Internal ID21454561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65052550..65056796hg38UCSC Ensembl
chr11:64820022..64824268hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384247
hg194247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603193
Supporting Variants
SamplesHG02011
Known GenesNAALADL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075265
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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