A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704012



Internal ID21225820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134665249..134665671hg38UCSC Ensembl
chr7:134350001..134350423hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2815540
Supporting Variants
Samples
Known GenesBPGM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704012
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.71875


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