A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585076



Internal ID20958147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76058095..76059170hg38UCSC Ensembl
chr17:74054176..74055251hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243183
Samples
Known GenesSRP68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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