A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704932



Internal ID21377208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055627..91055947hg38UCSC Ensembl
chr10:92815384..92815704hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389497
Supporting Variants
Samples
Known GenesLINC00502
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704932
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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