A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711379



Internal ID21233140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3146201..3146307hg38UCSC Ensembl
chr6:3146435..3146541hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814493
Supporting Variants
Samples
Known GenesBPHL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711379
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.642857


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