A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429270



Internal ID22487140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105535170..105535170hg38UCSC Ensembl
chr4:106456327..106456327hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429270
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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