A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414008



Internal ID22149371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1010982..1011255hg38UCSC Ensembl
chr10:1056922..1057195hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209700
Supporting Variants
SamplesHG00514
Known GenesGTPBP4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414008
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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