A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505752



Internal ID22563696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39953152..39963946hg38UCSC Ensembl
chr6:39920891..39931685hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3810795
hg1910795
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505752
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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