A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766491



Internal ID22100968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68277225..68277292hg38UCSC Ensembl
chr12:68671005..68671072hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766491
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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