A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865170



Internal ID22640105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34687965..34720147hg38UCSC Ensembl
chr10:34976893..35009075hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3832183
hg1932183
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461793
Samples
Known GenesPARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865170
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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