A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14401445



Internal ID22314982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68238792..68238855hg38UCSC Ensembl
chr7:67703779..67703842hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172711
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14401445
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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