A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064721



Internal ID21448529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31803349..31803410hg38UCSC Ensembl
chr1:32268950..32269011hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575214
Supporting Variants
SamplesHG00864
Known GenesSPOCD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064721
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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