A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762411



Internal ID22096913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98152355..98152627hg38UCSC Ensembl
chr10:99912112..99912384hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440049
Supporting Variants
Samples
Known GenesR3HCC1L
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762411
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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