A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449413



Internal ID22507283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72043662..72043662hg38UCSC Ensembl
chr6:72753365..72753365hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956525
Supporting Variants
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449413
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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