A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428220



Internal ID22486090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151140577..151140577hg38UCSC Ensembl
chr5:150520138..150520138hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952469
Supporting Variants
Samples
Known GenesANXA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428220
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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