A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560844



Internal ID20933915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36392203..36392539hg38UCSC Ensembl
chr6:36359980..36360316hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270707
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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