A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230961



Internal ID22372087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88592571..88627814hg38UCSC Ensembl
Outerchr9:91207486..91242729hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283534
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230961
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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