A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14441035



Internal ID22237481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110310153..110310233hg38UCSC Ensembl
chr1:110852775..110852855hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174209
Supporting Variants
SamplesHG00733
Known GenesLOC440600
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14441035
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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