A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578906



Internal ID20951977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64468315..64469128hg38UCSC Ensembl
chr17:62464432..62465245hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242653
Samples
Known GenesMILR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578906
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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