A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703770



Internal ID21376046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41870574..41870728hg38UCSC Ensembl
chr6:41838312..41838466hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392351
Supporting Variants
Samples
Known GenesUSP49
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703770
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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