A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188365



Internal ID22340205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139769314..139769374hg38UCSC Ensembl
chr7:139469113..139469173hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14402621
SamplesNA19240
Known GenesHIPK2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188365
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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