A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864142



Internal ID22639077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132736047..132757028hg38UCSC Ensembl
chr10:134549551..134570532hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3820982
hg1920982
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455502
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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