A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504426



Internal ID22562369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2863399..2867609hg38UCSC Ensembl
chr6:2863633..2867843hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845116
Supporting Variants
Samples
Known GenesMGC39372
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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