A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8871n152



Internal ID22824574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155405904..155409670hg38UCSC Ensembl
chr7:155198599..155202365hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383767
hg193767
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3170846, nsv3179706
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8871n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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