A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14383090



Internal ID22317238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21350718..21351574hg38UCSC Ensembl
chr7:21390336..21391192hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182067
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14383090
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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