A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457592



Internal ID22515473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110131868..110133086hg38UCSC Ensembl
chr1:110674490..110675708hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381219
hg191219
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457592
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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