A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584607



Internal ID20957678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42005846..42006790hg38UCSC Ensembl
chr17:40157864..40158808hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242984
Samples
Known GenesDNAJC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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