A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174167



Internal ID22332679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44883796..44883848hg38UCSC Ensembl
chr7:44923395..44923447hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14427450
SamplesHG00514
Known GenesPURB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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