A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481794



Internal ID22539699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8264992..8268017hg38UCSC Ensembl
chr1:8325052..8328077hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg383026
hg193026
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481794
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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