A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580248



Internal ID20953319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30730674..30732073hg38UCSC Ensembl
chr16:30741995..30743394hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243510
Samples
Known GenesSRCAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580248
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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