A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505743



Internal ID22563687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39232623..39237651hg38UCSC Ensembl
chr6:39200399..39205427hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385029
hg195029
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505743
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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