A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762391



Internal ID22096889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6795184..6795314hg38UCSC Ensembl
chr10:6837146..6837276hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437812
Supporting Variants
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SUBSDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762391
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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