A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202968



Internal ID22352057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88283210..88283268hg38UCSC Ensembl
chr6:88992929..88992987hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8005n152
Supporting Variantsnssv14467513
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202968
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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