A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829213



Internal ID22604148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225578984..225588527hg38UCSC Ensembl
chr1:225766686..225776229hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg389544
hg199544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466507
Samples
Known GenesENAH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829213
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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