A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855749



Internal ID22630684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96845480..96862646hg38UCSC Ensembl
chr10:98605237..98622403hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3817167
hg1917167
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459689
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855749
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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