A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454004



Internal ID22511879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105262358..105281616hg38UCSC Ensembl
chr1:105804980..105824238hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3819259
hg1919259
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454004
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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