A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151125



Internal ID21512627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52055237..52071310hg38UCSC Ensembl
chr6:51920035..51936108hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3816074
hg1916074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671293
Supporting Variants
Samples
Known GenesPKHD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151125
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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