A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571760



Internal ID20944831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142969329..142969798hg38UCSC Ensembl
chr6:143290466..143290935hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273139
Samples
Known GenesLOC100507489
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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