A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895584



Internal ID22670668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99942632..99943540hg38UCSC Ensembl
chr3:99661476..99662384hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428332
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895584
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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