A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182409



Internal ID22337086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44871104..44871178hg38UCSC Ensembl
chr7:44910703..44910777hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435877, nssv14377145, nssv14456338
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182409
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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