A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767369



Internal ID22101841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168940100..168940176hg38UCSC Ensembl
chr6:169340195..169340271hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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