A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171157



Internal ID22331137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98841712..98841849hg38UCSC Ensembl
chr2:99458175..99458312hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453875
SamplesHG00733
Known GenesKIAA1211L
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171157
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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