A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375797



Internal ID22295747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:881582..881656hg38UCSC Ensembl
chr11:881582..881656hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228754
Supporting Variants
SamplesNA19240
Known GenesCHID1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375797
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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