A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590300



Internal ID20963371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35783076..35784266hg38UCSC Ensembl
chr17:34110080..34111270hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242168
Samples
Known GenesMMP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590300
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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