A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451268



Internal ID22509140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39065271..39073782hg38UCSC Ensembl
chr1:39530943..39539454hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg388512
hg198512
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830310
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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