A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061271



Internal ID21452695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168584771..168584918hg38UCSC Ensembl
chr1:168554009..168554156hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579118
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061271
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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