A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937213



Internal ID21357283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3146427..3146630hg38UCSC Ensembl
chr6:3146661..3146864hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197232
SamplesHG002
Known GenesBPHL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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