A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595215



Internal ID20968286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73243701..73244338hg38UCSC Ensembl
chr17:71239840..71240477hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244574
Samples
Known GenesC17orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595215
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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