A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505765



Internal ID22563709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41595431..41596665hg38UCSC Ensembl
chr6:41563169..41564403hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845504
Supporting Variants
Samples
Known GenesFOXP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505765
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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