A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176955



Internal ID22334161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234644455..234650614hg38UCSC Ensembl
chr2:235553099..235559258hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg386160
hg196160
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5055n152
Supporting Variantsnssv14466465, nssv14457583
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176955
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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