A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111210



Internal ID21468112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209505632..209505755hg38UCSC Ensembl
chr2:210370356..210370479hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568497
Supporting Variants
SamplesHG03125
Known GenesMAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111210
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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