A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571617



Internal ID20944688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11916472..11917662hg38UCSC Ensembl
chr6:11916705..11917895hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6059n223
Supporting Variantsnssv18268614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571617
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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