A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14264379



Internal ID22202935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:109929060..110398674hg38UCSC Ensembl
Outerchr2:110686637..111156251hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38469615
hg19469615
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210360
Supporting Variants
SamplesHG00732
Known GenesLIMS3-LOC440895, LINC00116, LINC01106, LINC01123, LOC100288570, LOC100507334, LOC440895, MALL, MIR4267, MIR4436B1, MIR4436B2, NPHP1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14264379
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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