A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501777



Internal ID22559716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1393071..1394270hg38UCSC Ensembl
chr6:1393306..1394505hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844618
Supporting Variants
Samples
Known GenesFOXF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501777
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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