A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704055



Internal ID21376331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16132149..16134447hg38UCSC Ensembl
chr7:16171774..16174072hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382299
hg192299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392866
Supporting Variants
Samples
Known GenesISPD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704055
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.545977


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