A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061145



Internal ID21402386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150728630..150728805hg38UCSC Ensembl
chr1:150701106..150701281hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574989
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061145
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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