A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066372



Internal ID21434619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65670029..65670359hg38UCSC Ensembl
chr1:66135712..66136042hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577688
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066372
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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