A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746639



Internal ID21388429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815521..4815983hg38UCSC Ensembl
chr10:4857713..4858175hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431338
Supporting Variants
SamplesNB07
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746639
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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