A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830441



Internal ID22605376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70778190..70783889hg38UCSC Ensembl
chr1:71243873..71249572hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830441
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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