A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504333



Internal ID22562276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23101223..23104470hg38UCSC Ensembl
chr6:23101451..23104698hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383248
hg193248
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504333
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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