A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14437871



Internal ID22180965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:497801..509450hg38UCSC Ensembl
chr7:537438..549087hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3811650
hg1911650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201436
Supporting Variants
SamplesHG00514
Known GenesPDGFA
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14437871
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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