A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14462657



Internal ID22215203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155205203..155205203hg38UCSC Ensembl
chr7:154996913..154996913hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3540757
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14462657
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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