A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829118



Internal ID22604053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193105520..193108654hg38UCSC Ensembl
chr1:193074650..193077784hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg383135
hg193135
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464750
Samples
Known GenesGLRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829118
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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