A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359202



Internal ID22584871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21677740..21677740hg38UCSC Ensembl
chr10:21966669..21966669hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964742
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359202
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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