A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582157



Internal ID20955228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39445564..39446153hg38UCSC Ensembl
chr17:37601817..37602406hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242923
Samples
Known GenesMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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