A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415134



Internal ID22473004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109783812..109783812hg38UCSC Ensembl
chr4:110704968..110704968hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956046
Supporting Variants
Samples
Known GenesCFI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415134
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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