A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14277409



Internal ID22192931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:48491739..48570556hg38UCSC Ensembl
Outerchr7:48531335..48610152hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3878818
hg1978818
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220748
Supporting Variants
SamplesHG00731
Known GenesABCA13
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14277409
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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