A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14401834



Internal ID22320643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725414..77725472hg38UCSC Ensembl
chr7:77354731..77354789hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183680
Supporting Variants
SamplesNA19240
Known GenesRSBN1L
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14401834
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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