A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3542462



Internal ID22411539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708185..165708185hg38UCSC Ensembl
chr1:165677422..165677422hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440661
SamplesHG00733
Known GenesLOC440700
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3542462
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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