A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14374689



Internal ID22321126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141731723..141731880hg38UCSC Ensembl
chr7:141431523..141431680hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188283
Supporting Variants
SamplesNA19240
Known GenesWEE2-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14374689
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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