A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481095



Internal ID22538999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61557891..61562890hg38UCSC Ensembl
chr1:62023563..62028562hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481095
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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