A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225384



Internal ID22368529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74122904..74129627hg38UCSC Ensembl
Outerchr9:76737820..76744543hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386724
hg196724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282801, nssv14282800
SamplesHG00512, HG00731
Known GenesMIR6130
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225384
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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