A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14446768



Internal ID22242432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37729966..37729966hg38UCSC Ensembl
chr17:36089957..36089957hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3545446
Supporting Variants
SamplesHG00733
Known GenesHNF1B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14446768
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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