A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834030



Internal ID22608965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77130270..77141484hg38UCSC Ensembl
chr2:77357396..77368610hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3811215
hg1911215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488063
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834030
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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