A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434125



Internal ID21396127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99945041..99946577hg38UCSC Ensembl
chr3:99663885..99665421hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753538
SamplesNB07
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434125
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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