A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075895



Internal ID21415520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75763434..75763434hg38UCSC Ensembl
chr11:75474479..75474479hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659149
Supporting Variants
SamplesHG00731
Known GenesLOC283214
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075895
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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