A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590663



Internal ID20963734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7744309..7745087hg38UCSC Ensembl
chr17:7647627..7648405hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243233
Samples
Known GenesDNAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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