A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855661



Internal ID22630596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16670823..16714394hg38UCSC Ensembl
chr10:16712822..16756393hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3843572
hg1943572
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464240
Samples
Known GenesRSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855661
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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