A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14295609



Internal ID22264296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173737825..173738410hg38UCSC Ensembl
chr2:174602553..174603138hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558296
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14295609
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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