A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3535966



Internal ID22405205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64989892..64989892hg38UCSC Ensembl
chr4:65855610..65855610hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451824, nssv14424834
SamplesHG00733, HG00514
Known GenesLOC401134
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3535966
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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