A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177962



Internal ID22334727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214547168..214547219hg38UCSC Ensembl
chr2:215411892..215411943hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461986
SamplesHG00733
Known GenesVWC2L
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177962
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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