A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204495



Internal ID22353336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116357764..116357842hg38UCSC Ensembl
chr10:118117276..118117354hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14442059
SamplesHG00733
Known GenesCCDC172
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204495
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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