A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830169



Internal ID22605104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82554956..82559155hg38UCSC Ensembl
chr1:83020639..83024838hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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