A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115630



Internal ID21468073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85955780..85955927hg38UCSC Ensembl
chr2:86182903..86183050hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577578
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115630
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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