A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176908



Internal ID22334127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169554159..169554254hg38UCSC Ensembl
chr1:169523397..169523492hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv462n152
Supporting Variantsnssv14440687
SamplesHG00733
Known GenesF5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176908
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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