A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579267



Internal ID20952338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6492077..6492858hg38UCSC Ensembl
chr17:6395397..6396178hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2989n223
Supporting Variantsnssv18243305
Samples
Known GenesPITPNM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579267
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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