A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829488



Internal ID22604423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23315648..23317647hg38UCSC Ensembl
chr1:23642141..23644140hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456077
Samples
Known GenesHNRNPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829488
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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