A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754072



Internal ID21386807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7572795..7573673hg38UCSC Ensembl
chr10:7614758..7615636hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431380
Supporting Variants
SamplesMDQ025
Known GenesITIH5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754072
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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