A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576936



Internal ID20950007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58634915..58635561hg38UCSC Ensembl
chr17:56712276..56712922hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243038
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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