A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955368



Internal ID22730576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16209273..16209273hg38UCSC Ensembl
chr7:16248898..16248898hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435781
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955368
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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