A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065346



Internal ID21481961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42827203..42828899hg38UCSC Ensembl
chr1:43292874..43294570hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582520
Supporting Variants
SamplesHG03683
Known GenesERMAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065346
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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