A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451906



Internal ID22219368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87794711..87795385hg38UCSC Ensembl
chr4:88715863..88716537hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180590
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14451906
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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