A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830128



Internal ID22605063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67288146..67295164hg38UCSC Ensembl
chr1:67753829..67760847hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387019
hg197019
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830128
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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