A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412062



Internal ID22469932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16098767..16098767hg38UCSC Ensembl
chr5:16098876..16098876hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949931
Supporting Variants
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412062
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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