A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450375



Internal ID22508245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236957571..236969893hg38UCSC Ensembl
chr1:237120871..237133193hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3812323
hg1912323
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450375
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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