A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948534



Internal ID22724010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194311184..194311184hg38UCSC Ensembl
chr3:194028973..194028973hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427054
Samples
Known GenesLINC00887
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948534
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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