A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829932



Internal ID22604867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26511605..26525540hg38UCSC Ensembl
chr1:26838096..26852031hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3813936
hg1913936
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467457
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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