A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927577



Internal ID21347646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26611010..26617791hg38UCSC Ensembl
chr6:26611238..26618019hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386782
hg196782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197611
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927577
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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