A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577718



Internal ID20950789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18046645..18048046hg38UCSC Ensembl
chr17:17949959..17951360hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242097
Samples
Known GenesGID4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577718
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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