A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8748n152



Internal ID22824451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128798317..128799081hg38UCSC Ensembl
chr7:128438371..128439135hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3177876, nsv3171226, nsv3183619
SamplesNA19240, HG00733, HG00514
Known GenesCCDC136
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8748n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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