A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362857



Internal ID22588526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234669966..234669966hg38UCSC Ensembl
chr1:234805712..234805712hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362857
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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