A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501756



Internal ID22559695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137062146..137070304hg38UCSC Ensembl
chr6:137383283..137391441hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388159
hg198159
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844041
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501756
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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