A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828421



Internal ID22603356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17526228..17537165hg38UCSC Ensembl
chr1:17852724..17863660hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810938
hg1910937
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828421
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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