A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830347



Internal ID22605282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47175051..47178717hg38UCSC Ensembl
chr1:47640723..47644389hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg383667
hg193667
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830347
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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