A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063573



Internal ID21459546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2348735..2348800hg38UCSC Ensembl
chr1:2280174..2280239hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567888
Supporting Variants
SamplesHG02818
Known GenesMORN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063573
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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