A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281973



Internal ID22327459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91784941..91814409hg38UCSC Ensembl
Outerchr9:94547223..94576691hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3829469
hg1929469
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215786
Supporting Variants
SamplesNA19240
Known GenesROR2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281973
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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