A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706753



Internal ID21379029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105783380..105783787hg38UCSC Ensembl
chr2:106399837..106400244hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389845
Supporting Variants
Samples
Known GenesNCK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706753
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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