A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749260



Internal ID21388717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103895319..103908654hg38UCSC Ensembl
chr10:105655077..105668412hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3813336
hg1913336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431147
Supporting Variants
SamplesNB08
Known GenesOBFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749260
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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