A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485676



Internal ID22543587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150424261..150430685hg38UCSC Ensembl
chr3:150142048..150148472hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg386425
hg196425
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834711
Supporting Variants
Samples
Known GenesTSC22D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485676
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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