A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592976



Internal ID20966047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42035119..42035556hg38UCSC Ensembl
chr17:40187137..40187574hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242985
Samples
Known GenesZNF385C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592976
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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