A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190191



Internal ID22341144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120314130..120314246hg38UCSC Ensembl
chr7:119954184..119954300hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14401025
SamplesNA19240
Known GenesKCND2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190191
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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