A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466010



Internal ID22523901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26020233..26022432hg38UCSC Ensembl
chr1:26346724..26348923hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829806
Supporting Variants
Samples
Known GenesEXTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466010
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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