A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832101



Internal ID22607036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191130282..191133981hg38UCSC Ensembl
chr2:191995008..191998707hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488814
Samples
Known GenesSTAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832101
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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